Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8021957

FEI Number

3768

Entity Name

BIOMETRICS LTD.

City/State/Country

Newport Wales, GB

Establishment Address

NINE MILE POINT IND. ESTATE, UNITS 25-26,, Newport Wales NP11 7HZ, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BIOMETRICS LTD (Owner Number: 8021957)

Owner / Operator Contact Address

NINE MILE POINT IND. ESTATE, UNITS 25-26, NEWPORT, GB-NOTA NP11 7HZ, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K884003

PMA Number

N/A

All Registered Proprietary Names

PS900 Portable 8 Channel Goniometer & EMG System PS850 Portable 8 Channel EMG System K800 LS900 8 Channel Goniometer & EMG System LS1800 16 Channel EMG & Goniometer System PS800 Portable 8 Channel Goniometer System PS1800 Portable 16 Channel EMG & Goniometer System DataLOG PS1650 Portable 16 Channel EMG System LS800 8 Channel Goniometer System DS3000 Deluxe Data Acquisition System DS5000 Ultimate Data Acquisition System LS850 8 Channel EMG Ssytem LS1650 16 Channel EMG System MWX8 DataLINK DLK900 WK2 Wireless Kit 2 SX230-1000 EMG E-LINK M600 Exercise Kit SX230FW EMG GX3 EMG sensor DG1 Wireless Dongle X4 INTERX SX230 EMG WK1 Wireless Kit 1 WK0 Wirless Kit 0 GX4 EMG sensor GX5 Wireless EMG sensor SX230-100 EMG E-LINK M400 Exercsie Kit WK3 Wireless Kit 3 E-LINK M800 Wireless Exercise Kit E-LINK MYO-EX DG1 Wireless Dongle NC6 Large Wireless AngleX WK2 Wireless Kit 2 NC5 Samll Wireless AngleX NC3 Small AngleX NC4 Large AngleX WK0 Wirless Kit 0 WK3 Wireless Kit 3 E-LINK M400 Exercise Kit E-LINK M800 Wireless Exercise Kit E-LINK X4 InterX WK1 Wireless Kit 1 X4 INTERX E-LINK M600 Exercise kit E-LINK ANGLEX DLK900 MWX8 DataLOG DataLINK K800

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IKK	System, Isokinetic Testing And Evaluation	Physical Medicine	Class 2	890.1925	2008-04-11
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2007-04-27
BXB	Exerciser, Powered	Physical Medicine	Class 1	890.5380	2007-04-27
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2008-04-11

Official Correspondent

LINDA MILLER

US Agent Details

Linda Miller Business: Biometrics Ltd Email: lmiller@biometricsltd.com Phone: (804) 4482520

Related Public Records

Same Entity

BIOMETRICS 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
K873418	Bodylog, Inc.	BODYLOG STRESS REDUCTION PACKAGE	1987-12-17
K792659	Bio-Feedback Systems, Inc.	FEEDBACK EDR SYSTEM MODEL ME-1	1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8021957. Last updated year: 2026. Please use registration number 8021957 when referencing this establishment in official correspondence.