TS SA FIXTURE
Mexico·Clase III·IV. DENTAL SUPPLIES·HIOSSEN DE MÉXICO,S.A. DE C.V.·Registered May 21, 2021ELSISTEMAOSSTEMIMPLANTESTÁINDICADOPARAELUSOENMANDÍBULASYMAXILARESPARCIALOCOMPLETAMENTEEDÉNTULOS,ENAPOYO DE RESTAURACIONES UNITARIAS OMÚLTIPLES INCLUYENDO: RESTAURACIONESCON RETENCIÓNDEPRÓTESISCEMENTADA,RETENCIÓN ATORNILLADA OSOBREDENTADURAS,YSOPORTETEMPORALODEFINITIVOPARAUNPUENTEFIJO. COMORAÍZ DENTAL ARTIFICIAL PARA LARESTAURACIÓN DE DIENTES PERDIDOS, ELSISTEMA DE IMPLANTE OSSTEM IMPLANTESTÁDISEÑADOPARASUUSOENCIRUGÍADEIMPLANTE DENTAL; PUEDE SER IMPO
THE OSSTEMIMPLANT SYSTEM IS INDICATED FOR USE IN PARTIALLY OR COMPLETELY EDENTULOUS SYMAXILLARY JAWS, IN SUPPORT OF UNITARY OR MULTIPLE RESTORATIONS INCLUDING: RESTORATIONS WITH RETENTION OF CEMENTED PROSTHESIS, SCREWED RETENTION OR OVERDENTURES, AND TEMPORARY OR DEFINITIVE SUPPORT FOR A FIXED BRIDGE. AS AN ARTIFICIAL TOOTHROOT FOR THE RESTORATION OF MISSING TEETH, THE OSSTEM IMPLANT SYSTEM IS DESIGNED FOR USE IN DENTAL IMPLANT SURGERY; IT CAN BE IMPO
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- IV. INSUMOS DE USO ODONTOLÓGICO
- Product Type (English)
- IV. DENTAL SUPPLIES
- Trade Name (Spanish)
- SISTEMA DE IMPLANTE DENTAL INTRAÓSEO
- Trade Name (English)
- INTRAOSSEOUS DENTAL IMPLANT SYSTEM
- Analysis ID
- 876C2021 SSA
- Registration Date
- May 21, 2021
- Name (Spanish)
- HIOSSEN DE MÉXICO,S.A. DE C.V.
- Name (English)
- HIOSSEN DE MÉXICO,S.A. DE C.V.
Access comprehensive regulatory information for TS SA FIXTURE (TS SA FIXTURE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 876C2021 SSA and manufactured by HIOSSEN DE MÉXICO,S.A. DE C.V.. The device was registered on May 21, 2021.
This page provides complete registration details including product type (IV. DENTAL SUPPLIES), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.