# Pentron Corp.

- Location (FDA's records): Wallingford, CT
- FDA decisions: 15 (1984–2002): 15 510(k) clearances
- Product codes: EBF (10), KLE (2), EBC (1), EIH (1), EBG (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kerr Dental Materials Center: 1 (https://510kreport.com/company/kerr-dental-materials-center)

## Recent decisions
- K021457: Flex Span Temporary Crown & Bridge Material (Aug 1, 2002)
- K874189: Dual-Cure Radiopaque (Feb 11, 1988)
- K874275: Optec Supplementary Kit (Jan 19, 1988)
- K874162: Optec Stain Characterization and Modification Kit (Jan 12, 1988)
- K873683: Code #23 R System (Dentin Adhesive Material) (Nov 16, 1987)
- K873878: #24L System (Oct 27, 1987)
- K864404: Pentron High Strength Porcelain (Nov 24, 1986)
- K854803: Chameleon Bonding Kit (Mar 4, 1986)

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