# Anchor Innovation Medical (A.I.M.)

- Location (FDA's records): Rockville, MD
- FDA decisions: 2 (2014–2015): 2 510(k) clearances
- Product codes: GAT (1), GZB (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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.: 1 (https://510kreport.com/company/smith-nephew)
- Anulex Technologies, Inc.: 1 (https://510kreport.com/company/anulex-technologies)

## Firms that cite its devices most
- Stimwave Technologies Incorporated: 1 (https://510kreport.com/company/stimwave-technologies)

## Its most-cited devices
- K150924: A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device (2015), cited by 1

## Recent decisions
- K150924: A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device (Jul 27, 2015)
- K133770: A.I.M. Knotless Meniscal Repair Device (Jun 10, 2014)

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