American Dental Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K023547 | DIOLASE 980 D LASER SYSTEM | GEX | 2003-04-15 | View |
| 510(k) | K012127 | PULSEMASTER ERBIUM DENTAL LASER SYSTEM | GEX | 2001-10-04 | View |
| 510(k) | K012213 | GULLIVER AND CLASSE A | EIA | 2001-08-13 | View |
| 510(k) | K984486 | PULSEMASTER DENTAL LASER SYSTEM | GEX | 1999-05-13 | View |
| 510(k) | K972325 | PULSEMASTER 1000 ST DENTAL LASER SYSTEM | GEX | 1997-09-19 | View |
| 510(k) | K961269 | PULSEMASTER | GEX | 1997-03-10 | View |
| 510(k) | K961136 | PULSEMASTER | GEX | 1996-06-03 | View |
| 510(k) | K952333 | PLASMA ARC CURING SYSTEM | EBF | 1995-08-10 | View |
No matching devices.
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