# Ortho Source

- Location (FDA's records): North Hollywood, CA
- FDA decisions: 9 (1986–1992): 9 510(k) clearances
- Product codes: DYH (5), EBC (2), EMA (1), EJK (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Kay See Dental Mfg. Co.: 1 (https://510kreport.com/company/kay-see-dental-mfg)

## Its most-cited devices
- K861245: Orthosource Etch Systems (1986), cited by 1

## Recent decisions
- K913853: Fissure Sealer (Aug 27, 1992)
- K913854: Ortho Light Cure (Jan 14, 1992)
- K913519: Sumo Glass Ionomer Cement (Nov 19, 1991)
- K884949: Visible Light Cure Calcium Hydroxide Liner (Feb 23, 1989)
- K884575: Maxibond (Jan 3, 1989)
- K861118: Orthojoin, Orthodontic Adhesive (May 2, 1986)
- K861258: Permaband (Orthodontic Adhesive) (Apr 17, 1986)
- K861245: Orthosource Etch Systems (Apr 11, 1986)

Source page: https://510kreport.com/company/ortho-source