# Endolap, Inc.

- Location (FDA's records): Orlando, FL
- FDA decisions: 5 (1994–1997): 5 510(k) clearances
- Product codes: FAS (2), HET (1), HIF (1), GCJ (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
- K974515: Endolap Resectoscope Roller Electrode (Dec 22, 1997)
- K974516: Endolap Resectoscope Cutting Loop Electrode (Dec 22, 1997)
- K950243: Titan Insufflation Needle (Apr 6, 1995)
- K950219: Endolap Insufflator Tubing Set (Mar 23, 1995)
- K933492: Esys System (Mar 25, 1994)

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