Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015786035

FEI Number

3015786035

Entity Name

TUPEL LTD

City/State/Country

Oxford Oxfordshire, GB

Establishment Address

Magdalen Centre, 1 Robert Robertson Avenue, Oxford Oxfordshire ox4 4GA, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Tupel Ltd (Owner Number: 10083253)

Owner / Operator Contact Address

29 Eastern Avenue, Littlemore, Oxford, GB-OXF ox4 4qs, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tupel 3D Implant Scanner Tupel 3D Scan-Tracks

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOF	System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations	Dental	Class 2	872.3661	2021-11-08

Official Correspondent

Jonathan Mather

US Agent Details

Alan Rainbolt Business: BLUE SKY BIO, LLC Email: arainbolt@blueskybio.com Phone: (718) 3760422

Related Public Records

Same Entity

Tupel Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

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3044905014	FUSSEN IMAGING CO.,LTD.	Shenzhen Guangdong, CN
3010158379	DOF INC	Seoul, KR
3038590535	LARGEV INSTRUMENT CORP., LTD.	Beijing, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015786035. Last updated year: 2026. Please use registration number 3015786035 when referencing this establishment in official correspondence.