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“KEYSTONE” PrimaConnex Abutment - Taiwan Registration fcb5013fad94a6548f7dcedbff92842c

Access comprehensive regulatory information for “KEYSTONE” PrimaConnex Abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fcb5013fad94a6548f7dcedbff92842c and manufactured by Keystone Dental, Inc.. The authorized representative in Taiwan is HI-CLEARANCE INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KEYSTONE DENTAL, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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fcb5013fad94a6548f7dcedbff92842c
Registration Details
Taiwan FDA Registration: fcb5013fad94a6548f7dcedbff92842c
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Device Details

“KEYSTONE” PrimaConnex Abutment
TW: “凱石”牙科用植體基柱
Risk Class 2
MD

Registration Details

fcb5013fad94a6548f7dcedbff92842c

Ministry of Health Medical Device Import No. 028813

DHA05602881307

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3630 Dental bridges for bone explants

Imported from abroad

Dates and Status

Aug 29, 2016

Aug 29, 2026

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