# Tridak Division of Indicon, Inc.

- Location (FDA's records): Pearl River, NY
- FDA decisions: 7 (1984–1990): 7 510(k) clearances
- Product codes: FAP (2), FCW (1), FFS (1), KPI (1), HMX (1), HHT (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
- K891007: Nonimplanted Electrical Continence Device (Jun 7, 1990)
- K860744: Opthalmic Surgical Instruments (Mar 31, 1986)
- K853059: Laborie Fiberoptic Pressure Sensor & Interface (Jan 10, 1986)
- K852856: Laborie Urodynamics Processor (Oct 17, 1985)
- K851934: Cytological Cervical Spatula the Multi-Spatula (Jul 5, 1985)
- K842609: R.L. Medical Twin Light Source (Aug 9, 1984)
- K840605: Laborie Fibreoptic Light Cable (Apr 13, 1984)

Source page: https://510kreport.com/company/tridak-division-of-indicon