LAMBSMEAD LIMITED

FDA Device Registration & Listing · London London, City of, GB · Registration 3006123332

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
3006123332
FEI Number
3006123332
Entity Name
LAMBSMEAD LIMITED
City/State/Country
London London, City of, GB
Establishment Address
222 Upper Richmond Road West, London London, City of SW14 8AH, GB
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Lambsmead Limited (Owner Number: 9090360)
Owner / Operator Contact Address
222 Upper Richmond Road West, London, GB-LND SW14 8AH, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number

All Registered Proprietary Names

RESTYLANE INJECTABLE GEL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PKY Implant, Dermal, For Aesthetic Use In The Hands Unknown Class 3 N/A 2006-07-28
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2006-07-28

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Lambsmead Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006123332. Last updated year: 2026. Please use registration number 3006123332 when referencing this establishment in official correspondence.
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