# Endotherapeutics

- Location (FDA's records): Redwood City, CA
- FDA decisions: 7 (1984–1987): 7 510(k) clearances
- Product codes: HET (2), FHO (1), FAP (1), FBQ (1), FHP (1), GCP (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
- K870855: Uroscan (Jun 9, 1987)
- K860192: Endoport 5MM Single-Use Trocar and Sleeve (Mar 17, 1986)
- K860102: Mod. Endoneedle Single-Use Pneumoperitoneum Needle (Feb 12, 1986)
- K860103: Mod. Endoport Single-Use Trocar and Sleeve (Feb 12, 1986)
- K852031: Endoport 5MM (Aug 13, 1985)
- K844619: Endoneedle (Jan 9, 1985)
- K841716: Endoport Erocar (Jun 28, 1984)

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