FDA Device Establishments · JSON-LD · Markdown

PEARL INC.

FEI 3021887566 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3021887566
Owner / OperatorPearl Inc. (#10084584)
Address9200 W Sunset Blvd Ste 430, West Hollywood, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MYN
Regulation § (21 CFR)892.2070
Proprietary namesSecond Opinion Pediatric; Second Opinion

External sources

Source: openFDA. Public-domain (CC0).