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GRYPHON™ ANCHOR WITH ORTHOCORD® - FDA Registration MDR-00851

Access comprehensive regulatory information for GRYPHON™ ANCHOR WITH ORTHOCORD® in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00851 and manufactured by Depuy Mitek, Inc. 325 Paramaount Drive Raynham, MA 02767, USA Mfd By: Medos SARL Rue Du Puits Godet 20, Neuchatel CH - 2000, Switzerland in USA. The device was registered on December 18, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Phils.), Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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MDR-00851
GRYPHON™ ANCHOR WITH ORTHOCORD®
Registered medical device in Philippines
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Device Information
Product Name
GRYPHON™ ANCHOR WITH ORTHOCORD®
Registration Number
MDR-00851
Importer & Distribution
Registration Dates
Issuance Date
December 18, 2024
Expiry Date
September 20, 2028