FIRSTKIND LTD

FDA Device Registration & Listing · High Wycombe Buckinghamshire, GB · Registration 3011197543

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3011197543
FEI Number
3011197543
Entity Name
FIRSTKIND LTD
City/State/Country
High Wycombe Buckinghamshire, GB
Establishment Address
Suite 3, St Johns Court, Easton Street, High Wycombe Buckinghamshire HP11 1JX, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Firstkind Ltd (Owner Number: 10047447)
Owner / Operator Contact Address
Suite 3, St John's Court, Easton Street, High Wycombe, GB-BKM HP11 1JX, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

geko T-3 A-2 firefly T-2 geko T-2 geko T-3 geko W-3 firefly K-1 geko K-1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2018-05-30
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2022-05-05
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2020-06-19
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2023-05-17
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2022-05-04
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2022-05-05

Official Correspondent

Neil Buckley

US Agent Details

Sheila Hemeon-Heyer Business: Heyer Regulatory Solutions Email: sheila@heyer-regulatory.com Phone: (413) 3308578

Related Public Records

Same Entity

Firstkind 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
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011197543. Last updated year: 2026. Please use registration number 3011197543 when referencing this establishment in official correspondence.
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