# Heraeus Lasersonics, Inc.

- Location (FDA's records): Milpitas, CA
- FDA decisions: 38 (1988–1994): 38 510(k) clearances
- Product codes: GEX (37), HQF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K933245: Ultraline II Sterile Disposable Fiber (Apr 21, 1994)
- K923896: Hercules Model 5060 and 5100 ND:Yag Laser Systems (Nov 25, 1992)
- K921807: Ultraline Sterile Disposable Fiber (Jun 18, 1992)
- K915578: ND;Yag Surgical Laser Systems (Jun 15, 1992)
- K915583: CO2 Laser and Waveguide Delivery Systems for Thor. (Mar 27, 1992)
- K912618: Laser Systems for Percutaneous Lumbar Discectomy (Feb 27, 1992)
- K913887: C02 Laser Waveguide (Dec 9, 1991)
- K910530: Carbon Dioxide Laser Systems W/Waveguide Delivery (Oct 31, 1991)

Source page: https://510kreport.com/company/heraeus-lasersonics
