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Data / Medical devices / United Kingdom / Lambsmead Limited

Lambsmead Limited: FDA-registered device maker in London London, City of, United Kingdom, 1 PMA approval

Lambsmead Limited is registered with the FDA (registration 3006123332) in London London, City of, United Kingdom. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated March 25, 2005. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3006123332
Address
222 Upper Richmond Road West, London London, City of, United Kingdom, SW14 8AH
Owner or operator
Lambsmead Limited (9090360)
Roles
Exporter to the US
First device listed
July 28, 2006
Registered through
2027
Brand names listed
RESTYLANE INJECTABLE GEL

Devices it lists

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
March 25, 2005P040024RESTYLANE INJECTABLE GELLMH132March 12, 2026accessdata.fda.gov

Compare with other makers

Updated March 12, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.