Sunrise Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 18 products
Advertisement
Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K962192 | SUNRISE CURING LAMP | EBF | 1996-09-03 | View |
| 510(k) | K942542 | SLASE 210 PLUS HOLMIUM LASER SYSTEM | GEX | 1994-09-01 | View |
| 510(k) | K932997 | MICROPREP CAVITY PREPERATION SYSTEM | KOJ | 1994-04-25 | View |
| 510(k) | K933007 | SLASE 210 & SLASE 210 PLUS HOLMIUM LASER SYSTEMS | GEX | 1994-01-10 | View |
| 510(k) | K933017 | MODEL 5030 SUCTION HANDPIECE SYSTEM | GEX | 1993-07-26 | View |
| 510(k) | K931774 | UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER | GEX | 1993-07-22 | View |
| 510(k) | K930879 | 2.5 WATT PULSED DENTAL LASER SYSTEM | GEX | 1993-05-21 | View |
| 510(k) | K930789 | 8-WATT PULSED DENTAL LASER SYSTEM | GEX | 1993-05-21 | View |
| 510(k) | K925549 | SLASE 210 PLUS HOLMIUM LASER SYSTEM | GEX | 1993-03-09 | View |
| 510(k) | K920248 | MODEL SLASE 210 HOLMIUM LASER SYSTEM | GCX | 1992-07-21 | View |
| 510(k) | K920107 | ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR | GEX | 1992-03-13 | View |
| 510(k) | K920106 | ADL 400 ND;YAG LASER SYSTEM FOR INTRORAL SOFT TIS. | GEX | 1992-03-13 | View |
| 510(k) | K912879 | MODEL SLASE 210 HOLMIUM (THC:YAG) LASER SYSTEM | GEX | 1992-02-21 | View |
| 510(k) | K915352 | LASER FIBEROPTIC DELIVERY SYSTEM | GEX | 1991-12-17 | View |
| 510(k) | K914677 | MODEL DLASE 500 ND:YAG LASE SYS:INTRA SFT TIS SURG | GEX | 1991-11-08 | View |
| 510(k) | K914568 | MODEL DLASER 1000 ND;YAG LASER SYSTEM | GEX | 1991-11-07 | View |
| 510(k) | K913488 | STI CONTACT 200 FIBEROPTIC DELIVERY SYSTEM | GEX | 1991-09-10 | View |
| 510(k) | K900539 | MODEL DLASE 300 ND:YAG LASER SYSTEM: INTRAORAL | GEX | 1990-05-03 | View |
No matching devices.
Advertisement