# Vesitec Medical, Inc.

- Location (FDA's records): Laguna Hills, CA
- FDA decisions: 3 (1993–1994): 3 510(k) clearances
- Product codes: JDR (2), KOA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Influence, Inc.: 3 (https://510kreport.com/company/influence)
- Louisville Laboratories, Inc.: 3 (https://510kreport.com/company/louisville-laboratories)
- Linvatec Corp.: 1 (https://510kreport.com/company/linvatec)

## Its most-cited devices
- K932925: Bone Anchor for Soft Tissue Attachment (1994), cited by 5
- K931181: Vesitec Suture Passer (1993), cited by 1
- K931182: Vesitec Drill Guide (1993), cited by 1

## Recent decisions
- K932925: Bone Anchor for Soft Tissue Attachment (Apr 26, 1994)
- K931182: Vesitec Drill Guide (Jun 9, 1993)
- K931181: Vesitec Suture Passer (May 12, 1993)

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