Data / Medical devices / United States / Brown Precision Inc
Brown Precision Inc: FDA-registered device maker in Huntsville, AL, United States, 1 510(k) clearance
Brown Precision Inc is registered with the FDA (registration 3007856226) in Huntsville, AL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 23, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007856226
- Address
- 90 Shields Rd, Huntsville, AL, United States, 35811
- Owner or operator
- Brown Precision Inc (10057558)
- Roles
- Manufacturer, Reprocessor
- First device listed
- April 24, 2018
- Registered through
- 2026
- Brand names listed
- Bone Plates
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer | KRO | 2 | Manufacturer, Reprocessor | 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 |
|---|---|---|---|---|---|---|
| July 23, 2008 | K081111 | LEGION HINGE KNEE SYSTEM | KRO | Substantially Equivalent | Smith & Nephew, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 23, 2008. 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.