FDA Registration Active 🇬🇧 United Kingdom

Blink Medical LTD

Reg #: 3013602181 · FEI: 3013602181 · Expires 2026
Products
35
Proprietary Names
13
Establishment Types
4
Classifications
35

Registration Details

Registration Name
Blink Medical LTD
Registration Number
3013602181
FEI Number
3013602181
Status
Active
Expiry Year
2026
Initial Importer
No
Address
Unit 40, Radway Road, Shirley
City
Solihull
Country
GB

Owner / Operator

Firm Name
Corza Medical, Inc.
Operator Number
2242450
Address
2755 Canyon Boulevard, 1st Floor
City
Boulder
State
CO
Postal Code
80302
Country
US
Correspondent
Alex Castillo

US Agent

Business Name
KATENA PRODUCTS, INC.
Contact Name
Ruth James
Address
4 Middlebury Blvd, Unit 1
City
Randolph
State
NJ
ZIP
07869
Country
US
Phone
513 4964470

Products

Device Name Product Code
Gauze/Sponge, Internal, X-Ray Detectable GDY
Dissector, Surgical, General & Plastic Surgery GDI
Caliper, Ophthalmic HOE
Scissors, General, Surgical LRW
Hook, Ophthalmic HNQ
Specula, Ophthalmic HNC
Holder, Needle, Gastroenterologic FHQ
Clamp, Eyelid, Ophthalmic HOD
Retractor, Ophthalmic HNI
Curette, Ophthalmic HNZ
Instrument, Manual, Surgical, General Use MDM
Tray, Surgical LRP
Surgical Eye Tray PZG
Marker, Sclera HMQ
Forceps, General & Plastic Surgery GEN
Marker, Ocular HMR
Dilator, Lachrymal HNW
Scissors, Ophthalmic HNF
General Purpose Instrument Tray PXV
Spatula, Ophthalmic HND
Probe, Lachrymal HNL
Forceps, Ophthalmic HNR
Gauze / Sponge,Nonresorbable For External Use NAB
Retractor GAD
Container, Specimen, Sterile FMH
Minor Surgical Procedures Tray PYB
Cannula, Ophthalmic HMX
Single Use Instrument Tray OJV
Spoon, Ophthalmic HNB
Clamp, Surgical, General & Plastic Surgery GDJ
Instrument, Surgical, Disposable KDC
Drape, Surgical, Exempt PUI
Handle, Scalpel GDZ
Depressor, Orbital HNX
Suture Removal Kit MCZ

Proprietary Names

Wright Fascia Needle Infant Speculum Temporal Speculum Castroviejo Lid Speculum GRAETHER INSTRUMENT WIPES, PVA SPONGE INSTRUMENT TIP GUARDS Blink GASS SCLERAL MARKER Punctal Gauge Eagle BLINK KATENA DISPOSABLES

Establishment Types

Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Medical Device