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.

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Dental implant suprastructure, temporary, preformed, single-use

MHRA Device ID: 80800•Ref: 80800

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

Manufacturer Information

Name

Zest Anchors, LLC

Address

2875 Loker Ave. East

Carlsbad, CA, United States

Created Date

May 14, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Other Products from Zest Anchors, LLC (10)

Other Products from Same Authorized Representative (10)

Dental implant suprastructure, temporary, preformed, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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