# Endovations

- Location (FDA's records): Camp Hill, PA
- FDA decisions: 38 (1986–1996): 38 510(k) clearances
- Names in FDA's records: Endovations (37); Endovations, Inc. (1)
- Product codes: OCZ (14), FGE (4), FBK (2), OCX (2), KNS (2), KNT (2), MNL (2), FCF (1), GCJ (1), FDI (1), GCP (1), KNW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 3 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Denver Biomaterials, Inc.: 1 (https://510kreport.com/company/denver-biomaterials)

## Its most-cited devices
- K874063: Enteron Abdominal Paracentesis Tray (1987), cited by 1

## Recent decisions
- K955413: Endovations Triple Lumen Balloon Dilatation Catheter (Feb 8, 1996)
- K942110: Inject-Snare (Oct 13, 1994)
- K944049: Oxygen Mouthguard (Oct 11, 1994)
- K934315: Endovations (R) .035 Pre-Cut Papillatome (Feb 28, 1994)
- K913841: 2 Lumen Endos Retro Cholangiopancrea Injec Cath (Oct 8, 1991)
- K913870: 5MM Microscissors (Sep 16, 1991)
- K911155: Oval Cup Biopsy Forcep (Aug 7, 1991)
- K892218: Endo-Sponge (May 31, 1989)

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