# Msi, Inc.

- Location (FDA's records): Tarpon Springs, FL
- FDA decisions: 3 (1995–2022): 3 510(k) clearances
- Names in FDA's records: Msi, Inc. (2); Msi (1)
- Product codes: DOX (1), DYB (1), GAW (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Surgical Specialties Corp. Dba Angiotech: 1 (https://510kreport.com/company/surgical-specialties-dba-angiotech)

## Recent decisions
- K211178: DURAMESH Mesh Suture (Sep 2, 2022)
- K960200: Introstat Lead Introducer (Jul 2, 1996)
- K944226: Msi Procedure Kit (Jun 21, 1995)

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