# Medical Engineering Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 28 (1977–1993): 28 510(k) clearances
- Product codes: FAD (5), LJE (3), FGB (3), FRL (2), DWS (2), LCJ (2), FAE (2), GCY (1), FAP (1), FEN (1), BTO (1), FFG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Cook Urological, Inc.: 1 (https://510kreport.com/company/cook-urological)
- Cabot Medical Corp.: 1 (https://510kreport.com/company/cabot-medical)

## Its most-cited devices
- K905289: Surgitek (R) Lubri-Flex (TM) Ureteral Stent (1991), cited by 2

## Recent decisions
- K934141: Stand Alone Cystometrogram (Nov 18, 1993)
- K905289: Surgitek (R) Lubri-Flex (TM) Ureteral Stent (Mar 13, 1991)
- K903448: Surgitek Tex-Span Textured Tissue Expander (Jan 14, 1991)
- K902773: Surgitek (R) Flexible Ureteroscopy Intro/Sheath Set (Jul 16, 1990)
- K884746: Surgitek Flat T-Span (Aug 10, 1989)
- K883274: Surgitek (R) Uroflow System (Feb 8, 1989)
- K881736: Surgitek CO2 Delivery System (Aug 11, 1988)
- K880802: Surgitek Articulating Ureteroscope Model SU-11 (May 26, 1988)

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