Pentron Clinical Technologies
13 FDA 510(k) clearances · Manufacturer
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| BUILD-IT LIGHT CURE (K091512) | Pentron Clinical Technologies | 2009-10-30 |
| LUTE-IT II VENEER CEMENT, MODEL NO6 (K081887) | Pentron Clinical Technologies | 2008-08-29 |
| RM BOND, MODEL J032 (K072830) | Pentron Clinical Technologies | 2007-12-04 |
| GENERATION 8 SE ADHESIVE (K072480) | Pentron Clinical Technologies | 2007-11-21 |
| ARTISTE SE FLOWABLE COMPOSITE, MODEL N280 (K072545) | Pentron Clinical Technologies | 2007-10-26 |
| NANO-BOND II ADHESIVE SYSTEM (K071500) | Pentron Clinical Technologies | 2007-08-10 |
| SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE (K060889) | Pentron Clinical Technologies | 2006-10-27 |
| CEMENT-IT ALL PURPOSE, MODEL N97 (K060698) | Pentron Clinical Technologies | 2006-05-10 |
| SIMILE FLOW (K052106) | Pentron Clinical Technologies | 2005-10-31 |
| AVANTE LED CURING UNIT, MODEL N44 (K052349) | Pentron Clinical Technologies | 2005-10-21 |
| FIBERFILL AGP (K023818) | Pentron Clinical Technologies | 2003-04-03 |
| FIBERFILL SGP (K023819) | Pentron Clinical Technologies | 2003-03-26 |
| TRIONOMER (K022150) | Pentron Clinical Technologies | 2002-08-21 |
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Every clearance here is in the API, with alerts when new ones post.