# Pentron Clinical Technologies

- Location (FDA's records): Wallingford, CT
- FDA decisions: 13 (2002–2009): 13 510(k) clearances
- Product codes: EMA (3), EBF (3), KIF (2), KLE (2), DYH (1), EBZ (1), EKM (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 10 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Jeneric/Pentron, Inc.: 2 (https://510kreport.com/company/jeneric-pentron)
- Sybron Dental Specialties, Inc.: 1 (https://510kreport.com/company/sybron-dental-specialties)
- 3M Unitek: 1 (https://510kreport.com/company/3m-unitek)
- Centrix, Inc.: 1 (https://510kreport.com/company/centrix)
- Pulpdent Corp.: 1 (https://510kreport.com/company/pulpdent)
- Coltene/Whaledent, Inc.: 1 (https://510kreport.com/company/coltene-whaledent)

## Firms that cite its devices most
- Pentron Clinical: 1 (https://510kreport.com/company/pentron-clinical)
- Meta Biomed Co., Ltd.: 1 (https://510kreport.com/company/meta-biomed)
- Dmg USA, Inc.: 1 (https://510kreport.com/company/dmg-usa)

## Its most-cited devices
- K060698: Cement-IT All Purpose, Model N97 (2006), cited by 2
- K072545: Artiste SE Flowable Composite, Model N280 (2007), cited by 1

## Recent decisions
- K091512: Build-IT Light Cure (Oct 30, 2009)
- K081887: Lute-IT II Veneer Cement, Model NO6 (Aug 29, 2008)
- K072830: RM Bond, Model J032 (Dec 4, 2007)
- K072480: Generation 8 SE Adhesive (Nov 21, 2007)
- K072545: Artiste SE Flowable Composite, Model N280 (Oct 26, 2007)
- K071500: Nano-Bond II Adhesive System (Aug 10, 2007)
- K060889: SE Epiphany Root Canal Sealant, Model N59SE (Oct 27, 2006)
- K060698: Cement-IT All Purpose, Model N97 (May 10, 2006)

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