# Surgitek Medical Engineering Corp.

- Location (FDA's records): Racine, WI
- FDA decisions: 11 (1990–1992): 11 510(k) clearances
- Product codes: FGE (2), FDX (1), OCZ (1), GCA (1), FBK (1), FCL (1), ODD (1), GEI (1), FAD (1), FFL (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
- K914504: Cytology Brush (Feb 18, 1992)
- K914495: E.R.C.P. Catheter (Jan 30, 1992)
- K914497: Biopsy Forceps (Jan 3, 1992)
- K914505: Stone Basket (Dec 9, 1991)
- K914503: Grasping Forceps (Dec 5, 1991)
- K914496: Sclerotherapy Needle (Dec 5, 1991)
- K913928: Surgitek (R) 4.5FR Lubri-Flex (TM) Ureteral Stent (Nov 19, 1991)
- K913294: Surgitek (R) Laparoscopic Cholangiogram Kit (Oct 4, 1991)

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