# Teledyne Water Pik

- Location (FDA's records): Fort Collins, CO
- FDA decisions: 9 (1989–1997): 9 510(k) clearances
- Product codes: EFS (5), ELW (2), EAG (1), JEQ (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
- K970594: Kalginate Impression Material (Mar 31, 1997)
- K952422: Elastic Impression Cream (Aug 29, 1995)
- K944162: Denar Accuceph Cephalometer Imaging System (Nov 29, 1994)
- K940288: Water Pik Sensonic Plaque Removal Instrument (May 26, 1994)
- K931380: Water Pik Plus Plaque Control System (Sep 20, 1993)
- K905188: Perio Pik (Feb 15, 1991)
- K900547: Water Pik (R) W/Add'l Claims (Jun 15, 1990)
- K895259: Pik Pocket (R), Model PP-3 (Nov 1, 1989)

Source page: https://510kreport.com/company/teledyne-water-pik