Data / Medical devices / United States / Starr Frame LLC
Starr Frame LLC: FDA-registered device maker in Richardson, TX, United States, 1 510(k) clearance
Starr Frame LLC is registered with the FDA (registration 3007130914) in Richardson, TX, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 10, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007130914
- Address
- 1401 N. Central Expressway Suite 112, Richardson, TX, United States, 75080
- Owner or operator
- Starr Frame LLC (10026252)
- Roles
- Specification developer
- First device listed
- June 24, 2008
- Registered through
- 2026
- Brand names listed
- Reinert Reduction Tools, Starr Frame, Starr Frame Half Pins
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Traction, Non-Powered | HST | 1 | Specification developer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Specification developer | accessdata.fda.gov |
| Pin, Fixation, Smooth | HTY | 2 | Specification developer | accessdata.fda.gov |
| Pin, Fixation, Threaded | JDW | 2 | Specification developer | 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 10, 2008 | K082017 | STARR FRAME STEINMANN PIN | HTY | Substantially Equivalent | Starr Frame, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Orthopedic Manual Surgical Instrument
- All makers of Pin, Fixation, Smooth
- All makers of Pin, Fixation, Threaded
- All makers of Apparatus, Traction, Non-Powered
Updated October 10, 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.