Pentron Clinical Technologies
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K091512 | BUILD-IT LIGHT CURE | EBF | 2009-10-30 | View |
| 510(k) | K081887 | LUTE-IT II VENEER CEMENT, MODEL NO6 | EMA | 2008-08-29 | View |
| 510(k) | K072830 | RM BOND, MODEL J032 | DYH | 2007-12-04 | View |
| 510(k) | K072480 | GENERATION 8 SE ADHESIVE | KLE | 2007-11-21 | View |
| 510(k) | K072545 | ARTISTE SE FLOWABLE COMPOSITE, MODEL N280 | EBF | 2007-10-26 | View |
| 510(k) | K071500 | NANO-BOND II ADHESIVE SYSTEM | KLE | 2007-08-10 | View |
| 510(k) | K060889 | SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE | KIF | 2006-10-27 | View |
| 510(k) | K060698 | CEMENT-IT ALL PURPOSE, MODEL N97 | EMA | 2006-05-10 | View |
| 510(k) | K052106 | SIMILE FLOW | EBF | 2005-10-31 | View |
| 510(k) | K052349 | AVANTE LED CURING UNIT, MODEL N44 | EBZ | 2005-10-21 | View |
| 510(k) | K023818 | FIBERFILL AGP | KIF | 2003-04-03 | View |
| 510(k) | K023819 | FIBERFILL SGP | EKM | 2003-03-26 | View |
| 510(k) | K022150 | TRIONOMER | EMA | 2002-08-21 | View |
No matching devices.
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