# Laparomed Corp.

- Location (FDA's records): Irvine, CA
- FDA decisions: 10 (1991–1994): 10 510(k) clearances
- Product codes: GEI (3), GCJ (2), FGE (1), GCS (1), MFJ (1), GCX (1), KCJ (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
- K934527: Fascia Stitcher (Feb 25, 1994)
- K930569: Laparomed Laparoscopic Retractor System (Apr 20, 1993)
- K921921: Catheter Cholangiography (Aug 17, 1992)
- K921053: Laparomed Ligating Loop (Aug 6, 1992)
- K921006: Laparoscopic Retractor System (Jul 28, 1992)
- K914066: Electrosurgical Cutting/Coagulation Device/Access (Nov 7, 1991)
- K910074: Laparomed Hook/Spatula Device (Jul 2, 1991)
- K910219: Laparomed Cholangiogram Device (Apr 8, 1991)

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