# Ipg Medical Corporation

- Location (FDA's records): Marlborough, MA
- FDA decisions: 3 (2024–2025): 3 510(k) clearances
- Names in FDA's records: Ipg Medical Corporation (2); Ipg Medical (1)
- Product codes: GEX (3)
- 510(k) review time since 2016: median 210 days, against 90 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- G.N.S Neolaser, Ltd.: 2 (https://510kreport.com/company/gns-neolaser)
- Gyrus Acmi, Inc.: 1 (https://510kreport.com/company/gyrus-acmi)

## Its most-cited devices
- K232568: IPG Medical Family of Thulium  Fiber Lasers, Surgical Fibers, and Accessories (2024), cited by 1

## Recent decisions
- K251100: Ipgtfl-02 (Sep 19, 2025)
- K233344: Regenalase Laser System (May 28, 2024)
- K232568: IPG Medical Family of Thulium  Fiber Lasers, Surgical Fibers, and Accessories (Mar 21, 2024)

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