TRULIFE, LTD.

FDA Device Registration & Listing · S. Yorkshire Sheffield, GB · Registration 3006979871

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
3006979871
FEI Number
3006979871
Entity Name
TRULIFE, LTD.
City/State/Country
S. Yorkshire Sheffield, GB
Establishment Address
41 Amos Road, S. Yorkshire Sheffield S9 1BX, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Trulife (Owner Number: 10025240)
Owner / Operator Contact Address
41 Amos Road (Off Meadowhall Rd), Sheffield, GB-SHF S9 1BX, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Matrix Matrix Raw Matrix Max Matrix SuperMax Matrix Max 2 M-Pace L-Pace A-Pace U-Pace Matrix composite strut

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2008-04-01
ITC Stirrup, External Brace Component Physical Medicine Class 1 890.3410 2017-03-23

Official Correspondent

Debbie Emsden

US Agent Details

Dannielle Rehbein Business: Trulife, Inc Email: drehbein@trulife.com Phone: (360) 5988996

Related Public Records

Same Entity

Trulife
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
8020869 TRULIFE LTD. DUBLIN 24, IE

Similar Registrations

Registration Number Establishment Name Location
3005088750 3M POLAND MANUFACTURING SP. Z O.O WROCLAW Dolnoslaskie, PL
3013001618 CAST21 INC. Evanston, IL, US
2184046 OSBORN MEDICAL CORPORATION CENTENNIAL, CO, US
3006137579 ALIGNMED INC. Irvine, CA, US
3018302791 PILAB S.A.S. Bogota, CO
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006979871. Last updated year: 2026. Please use registration number 3006979871 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.