HIT TEINYO Robot Group
A Zhuhai-registered robot group whose scope covers smart home device manufacturing, mechanical and electrical equipment manufacturing, general equipment manufacturing, Class I–III medical device production and sales, and goods and technology import and export. The supplier presents rehabilitation robots, smart nursing beds and AI-assisted health screening. Workshop location, capacity, model-linked tests and certificate originals are not established by this listing.
Rehab and care devices, as presented by the supplier.
Medical-series rehab robots
Supplier materials list 3D cervical rehab robot N901, joint rehab robot J901, post-op rehab J902, spine systems S901/S902 and a surgical robot system. These are described as medical-class products. Model numbers, indications, registered device class and certificate numbers are not established by this listing. Obtain model-linked medical-device registration for the exact product and market.
Smart nursing beds
TY-R / R2M / R2O smart nursing beds with timed turning, air-pressure therapy and alternating support are described. Electrical ratings, load, dimensions and medical-device status per model need confirmation before quoting.
AI health screening devices
T330 series (tongue / posture / vital-sign screening), sleep ring and EEG sleep recorder are presented as health assessment tools. Claims about disease risk screening change the regulatory category; keep disease-diagnosis wording out of buyer-facing copy unless a registered device supports it.
Wellness and home devices
Spine care devices (S305PR / S306SSP), graphene capsule (S350VHF), moxibustion robot (A301MOX), bio-energy device (S108BiO), eye massagers (C101/C102) and sleep pillows are presented as wellness or home products. Destination market, electrical safety and whether any medical claim is intended must be stated per SKU.
What the registry confirms, and what stays open.
Manufacturing clauses are in the registered scope
Registry wording includes 智能家庭消费设备制造, 机械电气设备制造, 家用电器制造, 通用设备制造（不含特种设备制造） and 第一类医疗器械生产. This supports describing the entity as having manufacturing in scope; it does not by itself confirm which site runs each line.
Licensed medical-device production is in scope
许可项目 include 第二类医疗器械生产, 第三类医疗器械生产 and 第三类医疗器械经营. These are licensed activities: the scope text allows them only when approved. Obtain the actual medical-device production licence / registration certificates for the exact models before claiming market access.
Goods and technology export is in the registered scope
Registry wording includes 货物进出口 and 技术进出口. The company may export in its own name. Confirm the exporter of record, Incoterms and payment account for each order in writing.
New registration — ask for operating evidence
The Zhuhai entity was registered on 10 January 2025 (former name 珠海哈工天愈机器人有限公司). A young registration is not a defect, but buyers should request dated workshop photos or a line video and references from completed orders rather than relying on years-in-business claims from brand materials.
Address form is an office unit, not a confirmed plant
The registered address is Room 402, 4/F, Comprehensive Building H, No. 288 Airport East Road, Sanzao Town, Jinwan District, Zhuhai. That form is consistent with an office or lab unit. Confirm who manufactures each model and where the production line sits.
Related-party court notices on the risk feed
The 2026-10-15 risk snapshot returned 3 peripheral risk items (court hearing notices involving an affiliated company) and 78 warning items (name change, capital change, investor and personnel changes). Self-risk count was zero. Disclose and ask what the group structure means for the contracting party.
Brand history is longer than this entity
Supplier brand materials describe a group history from about 2016 and multiple regional headquarters. The contracting entity on this listing is the Zhuhai company registered in 2025. Confirm in writing which legal entity manufactures, holds certificates, signs the contract and receives payment.
What was checked — and what the check found.
Registry read is not a factory audit or product certification. Rehabilitation robots, nursing beds and health-screening devices may fall under medical-device, electrical-safety, EMC, wireless or general product rules depending on the destination and on whether disease diagnosis or treatment is claimed. Certificates listed by the supplier without holder name, number and date are declared, not sighted. Ordinary wellness devices must not be given an assumed medical or CE claim.
A Zhuhai robot-group registration, with medical-device, manufacturing and export clauses.
The current registry name is 珠海哈工天愈机器人集团有限公司, an active other limited liability company registered on 10 January 2025 in Jinwan District, Zhuhai (former name 珠海哈工天愈机器人有限公司). HIT TEINYO Robot Group is the supplier-facing brand used in its materials.
The registered scope covers smart robots R&D and sales; smart home consumer device manufacturing and sales; mechanical equipment R&D, sales and leasing; mechanical and electrical equipment manufacturing and sales; home appliance R&D, sales and manufacturing; general equipment repair and manufacturing; Class I medical device production, sales and leasing; Class II medical device leasing and sales; AI industry application system integration; software; technical services; health consulting (non-clinical); and goods and technology import and export. Licensed items include Class II and Class III medical device production and Class III medical device trading.
The registered address is Room 402, 4/F, Comprehensive Building H, No. 288 Airport East Road, Sanzao Town, Jinwan District, Zhuhai. That declared form is an office unit, not a confirmed production plant. Registry snapshot as of 15 October 2025: zero self-risk items; three peripheral court-hearing notices involving an affiliated company; 78 warning items covering name, capital, investor and personnel changes. Social-insurance headcount was not returned in the feed.
A January 2025 registration, and the evidence still to collect.
Zhuhai entity registered
Current registry entry dated 10 January 2025; later renamed to group form.
Brand materials describe multi-city footprint
Supplier PDFs list Zhuhai as global HQ and other China and overseas offices. Legal-entity map not independently confirmed.
CMH listing
Registry and risk snapshot read 15 October 2026; listing opened on those facts.
Qualify the line and licences
Obtain workshop evidence, model sheets, medical-device licences/registrations with numbers and holders, and certificate originals.
Where the devices may fit, after model and market checks.
Clinics and rehab centres
Cervical, joint and spine rehab robots as presented for clinical use. Confirm registered device class, indications and service network for the destination market.
Elderly care and nursing homes
Smart nursing beds and monitoring devices. Confirm electrical safety, medical-device status and after-sales terms for institutional buyers.
Community health cabins / wellness retail
AI health screening and wellness devices. Keep disease-diagnosis wording out unless a registered device supports it; classify the SKU correctly.
Distributors and OEM buyers
Multi-SKU catalogue with home, wellness and medical tiers. Ask for a model-by-model compliance matrix before bundling SKUs into one quotation.
Sourcing guides for this category
The 27-Point China Factory Audit Checklist
Product Inspection in China Before Shipment: A Buyer's Guide
How to Request a Sample from a Chinese Factory (Without Getting Burned)
What Documents to Request From a Chinese Supplier Before Your First Order
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Frequently Asked Questions
Is this a verified manufacturing factory?
The CMH Verified badge here means the company registration and manufacturing clauses in the registered scope were read and checked. It is not an on-site factory audit and does not certify product performance or medical-device registration.
What products are on the listing?
Rehabilitation robots, smart nursing beds, AI health screening systems and wellness devices as presented by the supplier. Exact model numbers, registered device class and certificate numbers are not established by this page.
Where is the factory?
The registered address is Room 402, 4/F, Comprehensive Building H, Jinwan District, Zhuhai. That is a declared office-unit form, not a confirmed production site. Ask for workshop photos or a line video and confirm which entity manufactures each model.
Can the company export in its own name?
Yes, goods and technology import/export clauses are in the registered scope. Still confirm the exporter of record, Incoterms, payment account and any destination-market importer of record for each order.
Do these products need medical-device approval abroad?
Often yes if they diagnose, treat or prevent disease. Class depends on claims and destination. Request model-linked registrations (e.g. NMPA, FDA, CE MDR) with holder name, number and date. Supplier lists of CE/FDA/CFDA without originals are declared, not verified.
What about wellness devices with health claims?
Claims can change the regulatory category. A massage or sleep device with disease-treatment wording may be treated as a medical device. State intended use and claims per SKU before quoting overseas.
Why is the group history longer than the registration date?
Brand materials describe a longer group story. The contracting entity on this listing is the Zhuhai company registered in 2025. Confirm in writing which legal entity manufactures, holds certificates, contracts and receives payment.
Are efficacy figures on this page?
No. Supplier materials include outcome figures; this listing does not use them. Buyers should request model-linked third-party reports before relying on any performance number.
Talk to HIT TEINYO Robot Group directly.
Send the target market, intended care setting (home / clinic / hospital), model number, voltage and plug standard, and first-order quantity. Ask who manufactures each model, where the line is, which medical-device registration or listing the exact model holds in the destination market, and obtain certificate originals with holder name, number and date before an order.