# Theramicro

- Location (FDA's records): Cordova, TN
- FDA decisions: 5 (2025–2026): 5 510(k) clearances
- Names in FDA's records: Theramicro (4); TheraMicro (1)
- Product codes: QUW (3), MBI (2)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Xiros, Ltd.: 4 (https://510kreport.com/company/xiros)
- Arthrex, Inc.: 3 (https://510kreport.com/company/arthrex)
- In2bones USA, LLC: 1 (https://510kreport.com/company/in2bones-usa)
- International Life Sciences: 1 (https://510kreport.com/company/international-life-sciences)

## Its most-cited devices
- K251063: TekBrace Solo Soft Tissue Reinforcement Device (2025), cited by 2
- K261621: TekBrace Solo Soft Tissue Reinforcement Device (2026), cited by 1

## Recent decisions
- K263352: TeKBrace Knotless Anchor (Oct 21, 2026)
- K262729: TeKBrace Solo Soft Tissue Reinforcement Device (Aug 18, 2026)
- K261621: TekBrace Solo Soft Tissue Reinforcement Device (Jun 9, 2026)
- K253538: TeKBrace Knotless Anchor (Mar 6, 2026)
- K251063: TekBrace Solo Soft Tissue Reinforcement Device (May 30, 2025)

Source page: https://510kreport.com/company/theramicro