Hoya Conbio, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K083899 | REVLITE Q-SWITCHED ND:YAG LASER SYSTEM | GEX | 2009-06-01 | View |
| 510(k) | K073158 | SCULPTURE 2.94 ER:YAG SYSTEM | GEX | 2008-08-27 | View |
| 510(k) | K073332 | V-RASER DIODE LASER SYSTEM | GEX | 2008-02-14 | View |
| 510(k) | K063384 | DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980 | GEX | 2007-03-16 | View |
| 510(k) | K063834 | REVLITE C6 Q-SWITCHED ND:YAG LASER SYSTEM | GEX | 2007-01-25 | View |
| 510(k) | K063112 | REVLITE Q-SWITCHED ND:YAG LASER | GEX | 2006-12-01 | View |
| 510(k) | K060977 | MEDLITE C SERIES COMPRESSION TOOL AND HANDPIECE ATTACHMENT ACCESSORY, MODEL 659-0523 | GEX | 2006-05-24 | View |
No matching devices.
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