# Iconn Orthopedics, LLC

- Location (FDA's records): Birmingham, AL
- FDA decisions: 5 (2014–2018): 5 510(k) clearances
- Product codes: MBI (4), HWC (1)
- 510(k) review time since 2016: median 82 days, against 91 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (1 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
- Arthrex, Inc.: 3 (https://510kreport.com/company/arthrex)
- Smith & Nephew Inc., Endoscopy Div.: 1 (https://510kreport.com/company/smith-nephew-endoscopy-div)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)

## Its most-cited devices
- K132724: Iconn Answer Suture Anchor (2014), cited by 1

## Recent decisions
- K180670: ICONN Campbell Interference Screw (Dec 7, 2018)
- K182264: ICONN Revolution Knotless Suture Anchor (Oct 19, 2018)
- K181680: ICONN Answer II Suture Anchor (Aug 9, 2018)
- K172491: ICONN Square 2.5MM Suture Anchor (Nov 29, 2017)
- K132724: Iconn Answer Suture Anchor (Apr 17, 2014)

Source page: https://510kreport.com/company/iconn-orthopedics