# Linvatec Corporation D/B/A Conmed Linvatec

- Location (FDA's records): Largo, FL
- FDA decisions: 4 (2011–2013): 4 510(k) clearances
- Product codes: MBI (2), HBC (1), MAI (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 7 (1 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Linvatec Corp.: 3 (https://510kreport.com/company/linvatec)
- Conmed Linvatec: 2 (https://510kreport.com/company/conmed-linvatec)

## Firms that cite its devices most
- Conmed Corporation: 3 (https://510kreport.com/company/conmed)
- Responsive Arthroscopy, LLC: 2 (https://510kreport.com/company/responsive-arthroscopy)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Its most-cited devices
- K131035: Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MM (2013), cited by 4
- K112965: Nano Suture Anchor (2011), cited by 3

## Recent decisions
- K131035: Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MM (Jul 2, 2013)
- K130497: D4000 Drive System; D4000A Drive System with Irrigation (Mar 29, 2013)
- K121890: Genesys Pressft Suture Anchor (Aug 22, 2012)
- K112965: Nano Suture Anchor (Nov 2, 2011)

Source page: https://510kreport.com/company/linvatec-d-b-a-conmed-linvatec