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 Daavlin Co. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 17, 2007: 3 SERIES PHOTOTHERAPY CABINET.
| Date | Record | Source |
|---|---|---|
| Jan 17, 2007 | 3 SERIES PHOTOTHERAPY CABINETK063621 · FTC | 510(k) clearances |
| Aug 26, 1993 | PSORALITEK930856 · FTC | 510(k) clearances |
| Nov 25, 1985 | SPECTRA 724K854498 · FTC | 510(k) clearances |
| Jan 3, 1983 | UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305K828654 · | 510(k) clearances |
| Oct 5, 1982 | SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USEK827690 · | 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
