FDA Device Entity Profile: The Argen Corporation

Known Identifiers & Locations

FEI Numbers 2433919, 3013551048

Owner Operator Numbers 9021799

Locations Covered SAN DIEGO, CA, US; San Diego, CA, US

Registered Establishments (2)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
2433919	THE ARGEN CORPORATION	SAN DIEGO, CA, US	Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device	View Details
3013551048	The Argen Corporation	San Diego, CA, US	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

AvaSpecs compiles public data records from the FDA database. This compiled profile does not indicate endorsement, safety, clearance, approval, or compliance status. AvaSpecs is a private search index and is not affiliated with the FDA or any government agency.