Invacare UK Ltd.

FDA Device Registration & Listing · Bridgend, GB · Registration 3007582653

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
3007582653
FEI Number
3007582653
Entity Name
Invacare UK Ltd.
City/State/Country
Bridgend, GB
Establishment Address
Pencoed Technology Park, Bridgend CF35 5AQ, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Invacare Corporation dba Invacare America (Owner Number: 1525712)
Owner / Operator Contact Address
One Invacare Way, Elyria, OH 44035, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Glissando Mattress Invacare Essentials Mattress Invacare® Softform Premier Mattress Invacare® Solace Mattress

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2009-02-25

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@UL.com Phone: (512) 3279997

Related Public Records

Same Entity

Invacare Corporation dba Invacare America
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007231105 Invacare GmbH Isny Baden-Wurttemberg, DE
3008370501 Invacare Portugal, Lda Leca do Balio Porto, PT
2081283 FREEDOM DESIGNS, INC. SIMI VALLEY, CA, US
3004730072 ALBER GMBH ALBSTADT Baden-Wurttemberg, DE
1531186 INVACARE CORP. DBA INVACARE AMERICA ELYRIA, OH, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007582653. Last updated year: 2026. Please use registration number 3007582653 when referencing this establishment in official correspondence.
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