Sunrise Technologies, Inc.
Sunrise Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1996.
Top product codes for Sunrise Technologies, Inc.
Recent clearances by Sunrise Technologies, Inc.
- K962192 — SUNRISE CURING LAMP
- K942542 — SLASE 210 PLUS HOLMIUM LASER SYSTEM
- K932997 — MICROPREP CAVITY PREPERATION SYSTEM
- K933007 — SLASE 210 & SLASE 210 PLUS HOLMIUM LASER SYSTEMS
- K933017 — MODEL 5030 SUCTION HANDPIECE SYSTEM
- K931774 — UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER
- K930789 — 8-WATT PULSED DENTAL LASER SYSTEM
- K930879 — 2.5 WATT PULSED DENTAL LASER SYSTEM
- K925549 — SLASE 210 PLUS HOLMIUM LASER SYSTEM
- K920248 — MODEL SLASE 210 HOLMIUM LASER SYSTEM
- K920106 — ADL 400 ND; YAG LASER SYSTEM FOR INTRORAL SOFT TIS.
- K920107 — ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR
- K912879 — MODEL SLASE 210 HOLMIUM (THC:YAG) LASER SYSTEM
- K915352 — LASER FIBEROPTIC DELIVERY SYSTEM
- K914677 — MODEL DLASE 500 ND:YAG LASE SYS:INTRA SFT TIS SURG
- K914568 — MODEL DLASER 1000 ND; YAG LASER SYSTEM
- K913488 — STI CONTACT 200 FIBEROPTIC DELIVERY SYSTEM
- K900539 — MODEL DLASE 300 ND:YAG LASER SYSTEM: INTRAORAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.