# Unisurge, Inc.

- Location (FDA's records): Cupertino, CA
- FDA decisions: 12 (1992–1994): 12 510(k) clearances
- Product codes: GCJ (10), GDO (1), HET (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
- K943502: Unigrip (Oct 7, 1994)
- K933720: Instrument Actuating Device (Iad) (Nov 12, 1993)
- K930605: Applier, Surgical, Clip (Oct 8, 1993)
- K930617: Obgrip and Unitips (TM) (Aug 11, 1993)
- K932604: Unigrip-FH Surgical Handpiece/Laparoscopic (Aug 10, 1993)
- K925882: Unitips Surgical Instruments (Aug 10, 1993)
- K930809: Unitips (Aug 10, 1993)
- K925917: Unichannel (TM Surgical Grasper (Aug 10, 1993)

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