Company ยท US
Theramicro
FDA 510(k) clearances and medical device recalls filed under this name, 2025 to 2026. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (4 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 21, 2026 | K263352 | TeKBrace Knotless Anchor TheraMicro | MBI |
| Aug 18, 2026 | K262729 | TeKBrace Solo Soft Tissue Reinforcement Device Theramicro | QUW |
| Jun 9, 2026 | K261621 | TekBrace Solo Soft Tissue Reinforcement Device Theramicro | QUW |
| Mar 6, 2026 | K253538 | TeKBrace Knotless Anchor Theramicro | MBI |
| May 30, 2025 | K251063 | TekBrace Solo Soft Tissue Reinforcement Device Theramicro | QUW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||