Jeneric/Pentron, Inc.
FDA 510(k) & PMA Approved Devices — 78 products
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Total Devices78
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K020499 | BOND-3 ADHESIVE | KLE | 2002-04-22 | View |
| 510(k) | K013543 | BOND-1 C & B | KLE | 2002-02-22 | View |
| 510(k) | K013542 | DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1) | KLE | 2002-02-14 | View |
| 510(k) | K012231 | AVANTE MICRO CRYSTAL SYSTEM | EIH | 2001-08-23 | View |
| 510(k) | K011748 | FIRST FILL R.C.S. | KIF | 2001-08-03 | View |
| 510(k) | K010957 | QUELL DESENSITIZER | LBH | 2001-06-25 | View |
| 510(k) | K011331 | JP CAST 40 | EJT | 2001-06-22 | View |
| 510(k) | K011330 | JP CAST 50 | EJT | 2001-06-22 | View |
| 510(k) | K011362 | GOLD CORE 73 LS | EJT | 2001-05-29 | View |
| 510(k) | K010044 | COSMIC | EJT | 2001-02-09 | View |
| 510(k) | K003683 | AVANTE CURELIGHT | EBZ | 2001-01-11 | View |
| 510(k) | K002854 | GOLD CORE POST SOLDER | EJT | 2000-12-20 | View |
| 510(k) | K002815 | GOLD CORE HF PRE SOLDER | EJT | 2000-12-19 | View |
| 510(k) | K003039 | GOLD CORE II | EJH | 2000-12-05 | View |
| 510(k) | K003037 | JEWEL CAST III | EJH | 2000-12-05 | View |
| 510(k) | K003011 | SELF ETCH BONDING PRIMER | KLE | 2000-11-28 | View |
| 510(k) | K001623 | SCULPTURE FLOW | EBF | 2000-07-11 | View |
| 510(k) | K001218 | CORRECT PLUS | ELW | 2000-07-05 | View |
| 510(k) | K001051 | RX EVEREST | EJT | 2000-04-28 | View |
| 510(k) | K994359 | BOND 1 C & B | KLE | 2000-03-21 | View |
No matching devices.
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