Pentron Clinical Technologies
Pentron Clinical Technologies holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2009.
Top product codes for Pentron Clinical Technologies
Recent clearances by Pentron Clinical Technologies
- K091512 — BUILD-IT LIGHT CURE
- K081887 — LUTE-IT II VENEER CEMENT, MODEL NO6
- K072830 — RM BOND, MODEL J032
- K072480 — GENERATION 8 SE ADHESIVE
- K072545 — ARTISTE SE FLOWABLE COMPOSITE, MODEL N280
- K071500 — NANO-BOND II ADHESIVE SYSTEM
- K060889 — SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE
- K060698 — CEMENT-IT ALL PURPOSE, MODEL N97
- K052106 — SIMILE FLOW
- K052349 — AVANTE LED CURING UNIT, MODEL N44
- K023818 — FIBERFILL AGP
- K023819 — FIBERFILL SGP
- K022150 — TRIONOMER
Data sourced from openFDA. This site is unofficial and independent of the FDA.