FDA Device Establishments · JSON-LD · Markdown

PROTECH PROFESSIONAL PRODUCTS, INC.

FEI 1000137415 · Manufacture Medical Device · Status: Active

FEI Number1000137415
Owner / OperatorPROTECH PROFESSIONAL PRODUCTS, INC. (#9006187)
Address2900 Commerce Park Dr Ste 10, BOYNTON BEACH, FL, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)EFT
Regulation § (21 CFR)872.3520
Proprietary namesSMILE AGAIN; PROTECH CONCENTRAT

External sources

Source: openFDA. Public-domain (CC0).