# Pentron Clinical

- Location (FDA's records): Orange, CA
- FDA decisions: 4 (2011–2013): 4 510(k) clearances
- Product codes: ELW (2), EBF (1), KLE (1)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 3 (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
- Jeneric/Pentron, Inc.: 4 (https://510kreport.com/company/jeneric-pentron)
- Heraeus Kulzer, Inc.: 2 (https://510kreport.com/company/heraeus-kulzer)
- Pentron Clinical Technologies: 1 (https://510kreport.com/company/pentron-clinical-technologies)
- Zhermack S.P.A.: 1 (https://510kreport.com/company/zhermack)
- Sybron Dental Specialties, Inc.: 1 (https://510kreport.com/company/sybron-dental-specialties)

## Firms that cite its devices most
- GC America, Inc.: 1 (https://510kreport.com/company/gc-america)
- Prevest Denpro Limited: 1 (https://510kreport.com/company/prevest-denpro)
- Millennium Company, LLC: 1 (https://510kreport.com/company/millennium)

## Its most-cited devices
- K102703: Build-IT Total Core (2011), cited by 2
- K120013: Tempspan Clear Matrix (2012), cited by 1

## Recent decisions
- K130920: Correct Plus 1 (Jul 2, 2013)
- K120013: Tempspan Clear Matrix (May 22, 2012)
- K111431: B1P Adhesive (Aug 1, 2011)
- K102703: Build-IT Total Core (Jan 5, 2011)

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