THETIS MEDICAL LTD.

FDA Device Registration & Listing · Godalming Surrey, GB · Registration 3022381831

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
3022381831
FEI Number
3022381831
Entity Name
THETIS MEDICAL LTD.
City/State/Country
Godalming Surrey, GB
Establishment Address
Park House, Stilemans, Hascombe Rd, Godalming Surrey GU84AB, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Thetis Medical Ltd. (Owner Number: 10084925)
Owner / Operator Contact Address
15 Leopold Street, Birmingham, GB-NOTA B12 0UP, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Thetis Medical Achilles Rupture Night Splint, Thetis Medical Achilles Rupture Trauma Splint

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FYH Splint, Extremity, Noninflatable, External, Sterile General, Plastic Surgery Class 1 878.3910 2022-04-15

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

Thetis Medical Ltd.
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 3022381831. Last updated year: 2026. Please use registration number 3022381831 when referencing this establishment in official correspondence.
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