# Lancer Orthodontics, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 14 (1990–2013): 14 510(k) clearances
- Product codes: EJF (7), DZE (1), DZB (1), NJM (1), EJJ (1), ELW (1), DYH (1), OAT (1)
- Predicates its devices cite: 4 (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

## Firms whose devices it cites most
- Jeil Medical Corporation: 1 (https://510kreport.com/company/jeil-medical)
- Sybron Dental Specialties, Inc.: 1 (https://510kreport.com/company/sybron-dental-specialties)
- Hdc Corp.: 1 (https://510kreport.com/company/hdc)
- T.O.a.D.S., LLC: 1 (https://510kreport.com/company/toads)

## Recent decisions
- K122069: Storm Mini Screw (Apr 11, 2013)
- K071192: Blugoo HD (Jun 22, 2007)
- K051552: O.a.S.I. System (Sep 19, 2005)
- K991481: Paragon (Aug 11, 1999)
- K904090: Orthodontic Bonding Adhesive Control (Apr 29, 1991)
- K904092: Lancer Original, Sierra, General Purpose (Nov 9, 1990)
- K904093: Buccal Tube, Buccal Attachment (Nov 7, 1990)
- K904091: Titanal,Sterling Spring,Dual Flex,Memorex,Bendallo (Nov 5, 1990)

Source page: https://510kreport.com/company/lancer-orthodontics