Data / Medical devices / United Kingdom / FAIRFAX MEDICAL PRODUCTS Ltd
FAIRFAX MEDICAL PRODUCTS Ltd: FDA-registered device maker in London London, City of, United Kingdom, 1 510(k) clearance
FAIRFAX MEDICAL PRODUCTS Ltd is registered with the FDA (registration 3004139812) in London London, City of, United Kingdom. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 3, 1991. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3004139812
- Address
- 40 ST Georges Road, London London, City of, United Kingdom, SW19 4ED
- Owner or operator
- Fairfax MEDICAL PRODUCTS Ltd (10035045)
- Roles
- Manufacturer
- First device listed
- January 28, 2011
- Registered through
- 2026
- Brand names listed
- Stabident, Stabilok, Stabilok drill
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Dental | DZM | 1 | Manufacturer | accessdata.fda.gov |
| Pin, Retentive And Splinting, And Accessory Instruments | EBL | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| June 3, 1991 | K910446 | STABIDENT LOCAL ANESTHESIA SYSTEM | DZM | Substantially Equivalent | Fairfax Dental, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Pin, Retentive And Splinting, And Accessory Instruments
- All makers of Drill, Dental, Intraoral
- All makers of Needle, Dental
Updated June 3, 1991. 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.