Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006803771

FEI Number

3006803771

Entity Name

CREST MEDICAL LIMITED

City/State/Country

Warrington Cheshire West and Chester, GB

Establishment Address

Unit 5, Farrell Industrial Estate; Howley Lane, Warrington Cheshire West and Chester WA1 2PB, GB

Establishment Type(s)

Foreign Private Label Distributor

Owner / Operator

Crest Medical Limited (Owner Number: 10061080)

Owner / Operator Contact Address

Unit 5, Farrell Industrial Estate, Howley Lane, Warrington, GB-WRT WA1 2PB, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ingrown Toe nail kit Toe Separator blanket protector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FZS	Curette, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2024-03-04
KIC	Cushion, Flotation	Physical Medicine	Class 1	890.3175	2022-06-14
FPY	Sheet, Burn	General Hospital	Class 1	880.5180	2022-05-29
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2019-08-13

Official Correspondent

Claire Deakin

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

Crest Medical Limited

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0034-2012	X Spine Systems Inc	1	Axle Interspinous Fusion System Torque Driver Handle, Model #: X060-0323, Lot # 525941, S/Ns 001-017, Lot # 525942, S/Ns 001-050, Mfr. By: Bradshaw Medical Inc., Kenosha, WI 53144 The Axle Torque Driver Handle is used to lock the set screw into the locking plate.

Similar Registrations

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8010298	RUDOLF MEDICAL GMBH + CO. KG	FRIDINGEN Baden-Wurttemberg, DE
3015895045	Sklar Corporation - Warehouse	Salisbury, MD, US
1038671	EXACTECH, INC.	GAINESVILLE, FL, US
9680735	HERMANN MUELLER Medizintechnik GmbH	TUTTLINGEN Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006803771. Last updated year: 2026. Please use registration number 3006803771 when referencing this establishment in official correspondence.