# Anchor Innovation Medical, Inc.

- Location (FDA's records): Rockville, MD
- FDA decisions: 1 (2013–2013): 1 510(k) clearance
- Product codes: MBI (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 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
- Smith & Nephew Inc., Endoscopy Division: 1 (https://510kreport.com/company/smith-nephew-endoscopy-division)
- Mitek Worldwide: 1 (https://510kreport.com/company/mitek-worldwide)

## Recent decisions
- K132461: A.I.M. Suture Anchor (Oct 16, 2013)

Source page: https://510kreport.com/company/anchor-innovation-medical