Pentron Clinical Technologies
FDA 510(k) medical device clearances.
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.