EMBOSS MEDICAL LIMITED

FDA Device Registration & Listing · London London, City of, GB · Registration 3017907745

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
3017907745
FEI Number
3017907745
Entity Name
EMBOSS MEDICAL LIMITED
City/State/Country
London London, City of, GB
Establishment Address
128 City Road, London London, City of EC1V 2NX, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Emboss Medical Limited (Owner Number: 10079807)
Owner / Operator Contact Address
27 Lantree Crescent, Cambridge, GB-LND CB2 9NJ, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K151095
PMA Number
N/A

All Registered Proprietary Names

Circumplast

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HFX Clamp, Circumcision Obstetrics/Gynecology Class 2 884.4530 2020-12-24

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

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017907745. Last updated year: 2026. Please use registration number 3017907745 when referencing this establishment in official correspondence.
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