Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Sunrise Technologies, Inc. with 18 510(k) clearances. The most recent is a 510(k) clearance dated Sep 3, 1996: SUNRISE CURING LAMP.
| Date | Record | Source |
|---|---|---|
| Sep 3, 1996 | SUNRISE CURING LAMPK962192 · EBF | 510(k) clearances |
| Sep 1, 1994 | SLASE 210 PLUS HOLMIUM LASER SYSTEMK942542 · GEX | 510(k) clearances |
| Apr 25, 1994 | MICROPREP CAVITY PREPERATION SYSTEMK932997 · KOJ | 510(k) clearances |
| Jan 10, 1994 | SLASE 210 & SLASE 210 PLUS HOLMIUM LASER SYSTEMSK933007 · GEX | 510(k) clearances |
| Jul 26, 1993 | MODEL 5030 SUCTION HANDPIECE SYSTEMK933017 · GEX | 510(k) clearances |
| Jul 22, 1993 | UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASERK931774 · GEX | 510(k) clearances |
| May 21, 1993 | 8-WATT PULSED DENTAL LASER SYSTEMK930789 · GEX | 510(k) clearances |
| May 21, 1993 | 2.5 WATT PULSED DENTAL LASER SYSTEMK930879 · GEX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
