Dental implant suprastructure, temporary, preformed, single-use - UK MHRA Medical Device Registration
Dental implant suprastructure, temporary, preformed, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 80800. The device is manufactured by Zest Anchors, LLC from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP LIMITED.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
General Medical Device
Devices
Dental implant suprastructure, temporary, preformed, single-use
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Feb 17, 2024
Address
2875 Loker Ave. East
Carlsbad, CA, United States
Created Date
May 14, 2021
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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Dental implant suprastructure, permanent, preformed
Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
Dental implant suprastructure, temporary, preformed, single-use
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Dental implant suprastructure, permanent, preformed
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Type: General Medical Device
Registered: Nov 26, 2024
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