Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005225959

FEI Number

3005225959

Entity Name

CAMBRIAN MEDICAL, INC.

City/State/Country

Cedar City, UT, US

Establishment Address

1719 S WESTVIEW DR, Cedar City, UT 84720, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

CAMBRIAN MEDICAL, INC (Owner Number: 9074465)

Owner / Operator Contact Address

1719 S WESTVIEW DR, Cedar City, UT 84720, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical Cambrian Medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical cambrian medical

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXB	Probe	Orthopedic	Class 1	888.4540	2012-01-19
EFL	Forceps, Dressing, Dental	Dental	Class 1	872.4565	2012-01-19
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2012-01-19
HNC	Specula, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-21
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2012-01-22
GAF	Spatula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2012-01-19
HOE	Caliper, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-21
HNG	Rongeur, Lachrymal Sac	Ophthalmic	Class 1	886.4350	2012-01-19
HXZ	Cutter, Wire	Orthopedic	Class 1	888.4540	2012-01-19
FZY	Hammer, Surgical	General, Plastic Surgery	Class 1	878.4800	2012-01-19
HNQ	Hook, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-22
HNW	Dilator, Lachrymal	Ophthalmic	Class 1	886.4350	2012-01-21
HMR	Marker, Ocular	Ophthalmic	Class 1	886.4570	2012-01-21
HRR	Scissors, Orthopedic, Surgical	Orthopedic	Class 1	888.4540	2012-01-19
HTX	Rongeur	Orthopedic	Class 1	888.4540	2012-01-19
FHQ	Holder, Needle, Gastroenterologic	Gastroenterology, Urology	Class 1	876.4730	2012-01-19
EHY	Tray, Impression, Preformed	Dental	Class 1	872.6880	2012-01-19
HNL	Probe, Lachrymal	Ophthalmic	Class 1	886.4350	2012-01-22
HNJ	Punch, Corneo-Scleral	Ophthalmic	Class 1	886.4350	2012-01-21
HTF	Curette	General, Plastic Surgery	Class 1	878.4800	2012-01-19
HMX	Cannula, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-21
HND	Spatula, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-21
HNF	Scissors, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-21
HNR	Forceps, Ophthalmic	Ophthalmic	Class 1	886.4350	2012-01-22
EKK	Spreader, Pulp Canal Filling Material, Endodontic	Dental	Class 1	872.4565	2012-01-19

Official Correspondent

ASITA PRABHUSHANKAR

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CAMBRIAN MEDICAL, INC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02
K871646	Ocular Instruments, Inc.	TANNE CORNEAL CUTTING BLOCK	1987-05-18
K854401	Microsurgical Technology, Inc.	THE NEW MOBILE TIP MCINTYRE CANNULA	1985-12-30

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
Z-0011-2019	Ellex iScience, Inc.	1	ellex I.Science iTRACK 250A, Canaloplasty Microcatheter Kit, for single use, REF iT-250A, Rx. The firm name on the label is Ellex iScience, Inc., Fremont, CA. Used in ophthalmic surgery.
Z-0022-2009	Becton Dickinson and Company	1	BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery.

Similar Registrations

Registration Number	Establishment Name	Location
2134947	GAUTHIER BIOMEDICAL, INC.	Grafton, WI, US
3004215117	MILLENNIUM SURGICAL CORP	Schaumburg, IL, US
1421879	PHOENIX INSTRUMENTS, INC.	Lisle, IL, US
3010155661	Synergy Health Sterilisation UK Ltd	Thorne Doncaster, GB
3015516266	Depuy Ireland UC	Co. Cork Munster, IE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005225959. Last updated year: 2026. Please use registration number 3005225959 when referencing this establishment in official correspondence.