# Ziptek, LLC

- Location (FDA's records): Sarasota, FL
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: MAI (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (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
- Arthrex, Inc.: 2 (https://510kreport.com/company/arthrex)
- Biomet Sports Medicine: 1 (https://510kreport.com/company/biomet-sports-medicine)

## Firms that cite its devices most
- Paragon 28, Inc.: 1 (https://510kreport.com/company/paragon-28)
- Conextions Medical: 1 (https://510kreport.com/company/conextions-medical)

## Its most-cited devices
- K162429: ZipE Knotless Tissue Repair and Attachment Devices (2017), cited by 2

## Recent decisions
- K162429: ZipE Knotless Tissue Repair and Attachment Devices (Mar 13, 2017)

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