Data / Medical devices / Hong Kong / Vincent Rehab Devices Company Limited
Vincent Rehab Devices Company Limited: FDA-registered device maker in Hongkong, Hong Kong, 3 510(k) clearances
Vincent Rehab Devices Company Limited is registered with the FDA (registration 3014301596) in Hongkong, Hong Kong. It lists 11 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 18, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014301596
- Address
- Flat/Rm B2,7/F,hang Fung Ind.bldg. Phase 2,2G Hok Yuen St,hung Hom,kowloon, Hongkong, Hong Kong, --
- Owner or operator
- VINCENT REHAB DEVICES COMPANY LIMITED (10053511)
- Roles
- Exporter to the US
- First device listed
- December 13, 2016
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bedding, Disposable, Medical | KME | 1 | Exporter to the US | accessdata.fda.gov |
| Device, Fixation, Tracheal Tube | CBH | 1 | Exporter to the US | accessdata.fda.gov |
| Joint, Ankle, External Brace | ITW | 1 | Exporter to the US | accessdata.fda.gov |
| Joint, Knee, External Brace | ITQ | 1 | Exporter to the US | accessdata.fda.gov |
| Orthosis, Limb Brace | IQI | 1 | Exporter to the US | accessdata.fda.gov |
| Orthosis, Lumbar | IQE | 1 | Exporter to the US | accessdata.fda.gov |
| Orthosis, Thoracic | IPT | 1 | Exporter to the US | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Exporter to the US | accessdata.fda.gov |
| Restraint, Protective | FMQ | 1 | Exporter to the US | accessdata.fda.gov |
| Support, Arm | IOY | 1 | Exporter to the US | accessdata.fda.gov |
| Support, Breathing Tube | JAY | 1 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 18, 1996 | K962834 | HEELBO QUILTED LIMB HOLDER WITH DOUBLE D-RING, QUICK-RELEASE SNAP, AND STRAP | FMQ | Substantially Equivalent | Heelbo, Inc. | accessdata.fda.gov |
| October 18, 1996 | K962831 | THE INCH QUILTED LIMB HOLDER WITH QUICK RELEASE SNAP CLOSURE | FMQ | Substantially Equivalent | Heelbo, Inc. | accessdata.fda.gov |
| October 9, 1996 | K962778 | THE L-BOW ARM RESTRAINT | FMQ | Substantially Equivalent | Heelbo, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Restraint, Protective
- All makers of Support, Breathing Tube
- All makers of Orthosis, Lumbar
- All makers of Orthosis, Limb Brace
- All makers of Orthosis, Thoracic
- All makers of Joint, Ankle, External Brace
Updated October 18, 1996. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.