Sunrise Technologies, Inc.
Mountain View, CA, US
Sunrise Technologies, Inc. appears in FDA device records in Mountain View, CA. FDA records list 18 510(k) clearances between and , 4 PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 18
- PMA records
- 4
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Sunrise Technologies, Inc. between 1990 and 1996. The busiest year on record is 1993, with 5. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 1 |
| 1991 | 4 |
| 1992 | 4 |
| 1993 | 5 |
| 1994 | 3 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K962192 | SUNRISE CURING LAMP | EBF | Substantially Equivalent | |
| K942542 | SLASE 210 PLUS HOLMIUM LASER SYSTEM | GEX | Substantially Equivalent | |
| K932997 | MICROPREP CAVITY PREPERATION SYSTEM | KOJ | Substantially Equivalent | |
| K933007 | SLASE 210 & SLASE 210 PLUS HOLMIUM LASER SYSTEMS | GEX | Substantially Equivalent | |
| K933017 | MODEL 5030 SUCTION HANDPIECE SYSTEM | GEX | Substantially Equivalent | |
| K931774 | UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER | GEX | Substantially Equivalent | |
| K930879 | 2.5 WATT PULSED DENTAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K930789 | 8-WATT PULSED DENTAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K925549 | SLASE 210 PLUS HOLMIUM LASER SYSTEM | GEX | Substantially Equivalent | |
| K920248 | MODEL SLASE 210 HOLMIUM LASER SYSTEM | GCX | Unknown | |
| K920107 | ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR | GEX | Substantially Equivalent | |
| K920106 | ADL 400 ND;YAG LASER SYSTEM FOR INTRORAL SOFT TIS. | GEX | Substantially Equivalent | |
| K912879 | MODEL SLASE 210 HOLMIUM (THC:YAG) LASER SYSTEM | GEX | Substantially Equivalent | |
| K915352 | LASER FIBEROPTIC DELIVERY SYSTEM | GEX | Substantially Equivalent | |
| K914677 | MODEL DLASE 500 ND:YAG LASE SYS:INTRA SFT TIS SURG | GEX | Substantially Equivalent | |
| K914568 | MODEL DLASER 1000 ND;YAG LASER SYSTEM | GEX | Substantially Equivalent | |
| K913488 | STI CONTACT 200 FIBEROPTIC DELIVERY SYSTEM | GEX | Substantially Equivalent | |
| K900539 | MODEL DLASE 300 ND:YAG LASER SYSTEM: INTRAORAL | GEX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain