FDA Device Establishments · JSON-LD · Markdown

BIOPHOTAS, INC.

FEI 3009765778 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3009765778
Owner / OperatorBioPhotas (#10041655)
Address15501 Red Hill Avenue, #200, Tustin, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)OAP
Regulation § (21 CFR)890.5500
Proprietary namesCelluma RESTORE; Celluma Series 2 NOVA; Celluma Series 2 ELITE; Celluma Series 2 CONTOUR PLUS; Celluma Series 2 RESTORE; Celluma MYSTIQUE

External sources

Source: openFDA. Public-domain (CC0).