Sunrise Technologies, Inc.
FDA 510(k) medical device clearances.
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.