Corza Medical, Inc.

Entity profile compiled from public source records

Public Record Profile Registrations: 8 510(k) filings: 0 Recalls: 0

Known Identifiers & Locations

FEI Numbers 2242450, 3001180016, 3002443341, 3007109793, 3010692967, 3011767135, 3013602181, 3015177648
Owner Operator Numbers 2242450, 9060279
Locations Covered Chula Vista, CA, US; Fenton, MO, US; Grand Blanc, MI, US; Parsippany, NJ, US; Randolph, NJ, US; Solihull, GB; Taunton Somerset, GB; Tijuana Baja California, MX

Registered Establishments (8)

Registration # Establishment Name Location Establishment Type(s) Action
1835993 BARRON PRECISION INSTRUMENTS, L.L.C. Grand Blanc, MI, US Manufacture Medical Device View Details
1934420 KATENA PRODUCTS, INC. Fenton, MO, US Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device View Details
2242450 KATENA PRODUCTS, INC. Randolph, NJ, US Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility View Details
3007109793 Surgical Specialties Corporation Limited (UK) Taunton Somerset, GB Manufacture Medical Device for Another Party (Contract Manufacturer) View Details
3010692967 Surgical Specialties Mexico S DE RL DE CV Tijuana Baja California, MX Manufacture Medical Device for Another Party (Contract Manufacturer) View Details
3011767135 SSC- Surgical Specialties Corporation Chula Vista, CA, US Complaint File Establishment per 21 CFR 820.198 View Details
3013602181 Blink Medical LTD Solihull, GB Repack or Relabel Medical Device,Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility View Details
3015177648 KATENA PRODUCTS, INC. Parsippany, NJ, US Develop Specifications But Do Not Manufacture At This Facility 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.

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