Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8020712

FEI Number

3008237817

Entity Name

LOCKDOWN MEDICAL LIMITED

City/State/Country

Redditch Worcestershire, GB

Establishment Address

16 The Oaks, Clews Road, Redditch Worcestershire B98 7ST, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lockdown Medical Ltd (Owner Number: 8020712)

Owner / Operator Contact Address

16 THE OAKS, CLEWS RD, --, REDDITCH, WORCESTERSHIRE, GB-BIR B98 7ST, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LockDown LockDown Lockdown Depth Gauge LockDown LockDown

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FTL	Mesh, Surgical, Polymeric	General, Plastic Surgery	Class 2	878.3300	2008-07-25
HCF	Instrument, Ligature Passing And Knot Tying	General, Plastic Surgery	Class 1	878.4800	2007-11-15
HTJ	Gauge, Depth	Orthopedic	Class 1	888.4300	2020-10-23
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2007-11-15
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2007-11-15

Official Correspondent

No official correspondent registered.

US Agent Details

Scott Baltsen Business: Lockdown Surgical Inc Email: scott.baltsen@lockdownsurgical.com Phone: (708) 4170775

Related Public Records

Same Entity

Lockdown Medical Ltd

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
K220540	Covidien	ProGrip Self-Gripping Polypropylene Mesh	2022-09-22

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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8020712. Last updated year: 2026. Please use registration number 8020712 when referencing this establishment in official correspondence.