# Kerr Corporation (Danbury)

- Location (FDA's records): Washington, DC
- FDA decisions: 32 (1978–2005): 32 510(k) clearances
- Product codes: KLE (7), EMA (4), ELW (3), EBF (3), EJJ (3), EJK (2), EGS (2), EBZ (2), EFD (1), EBC (1), EJR (1), EHY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Sterngold/Implamed: 3 (https://510kreport.com/company/sterngold-implamed)
- Eele Laboratories, LLC: 1 (https://510kreport.com/company/eele-laboratories)
- Kuraray America, Inc.: 1 (https://510kreport.com/company/kuraray-america)
- Kuraray Co.: 1 (https://510kreport.com/company/kuraray)
- (Ems Sa) Electro Medical Systems: 1 (https://510kreport.com/company/ems-sa-electro-medical-systems)
- Dmg USA, Inc.: 1 (https://510kreport.com/company/dmg-usa)
- Apoza Enterprise Co., Ltd.: 1 (https://510kreport.com/company/apoza-enterprise)
- Biomat Sciences, Inc.: 1 (https://510kreport.com/company/biomat-sciences)

## Its most-cited devices
- K940513: Optibond (1994), cited by 3
- K020091: Optilux 501 (2002), cited by 3
- K934690: Kerr Optibond, Modification (1993), cited by 2
- K894219: Temp Bond NE (1989), cited by 1
- K923546: Optibond (1992), cited by 1
- K844662: Kerr Herculite Dental Composite Restorative Materi (1985), cited by 1

## Recent decisions
- K051545: L.E. Demetron II (Jul 18, 2005)
- K020091: Optilux 501 (Mar 21, 2002)
- K951663: Tytin R (Jun 6, 1995)
- K951511: Tytin Admix (May 2, 1995)
- K942480: M4 Contra-Angle Handpiece (Jan 27, 1995)
- K940513: Optibond (Apr 15, 1994)
- K935535: TYTIN (Mar 11, 1994)
- K934690: Kerr Optibond, Modification (Dec 30, 1993)

Source page: https://510kreport.com/company/kerr-danbury