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MEDOS GRYPHON® P PEEK Anchor with DYNACORD™ Suture - HSA Registration DE0507740

Access comprehensive regulatory information for MEDOS GRYPHON® P PEEK Anchor with DYNACORD™ Suture in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0507740 and owned by Medos International SARL. The device was registered on February 03, 2023.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS C
DE0507740
MEDOS GRYPHON® P PEEK Anchor with DYNACORD™ Suture
HSA Registration Number: DE0507740
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Product Description

The GRYPHON Anchors with DYNACORD Suture are intended for use in soft tissue to bone reattachment. Shoulder: • Bankart Repair • SLAP Leison Repair • Capsular Shift or Capsulolabral Reconstruction

Device Classification
Device Class
CLASS C
Medical Speciality Area
Orthopaedics
Registration Information
Registration Number
DE0507740
Registration Date
February 03, 2023
Change Notification Approval Date
March 17, 2025
Retention Due Date
February 02, 2026
Product Owner
Short Name
Medos International SARL
Address
Chemin-Blanc 38, CH 2400, Le locle, SWITZERLAND
Registrant
Address
2 SCIENCE PARK DRIVE, ASCENT, #07-13, SINGAPORE 118222
Importer
Address
2 SCIENCE PARK DRIVE, ASCENT, #07-13, SINGAPORE 118222 2 SCIENCE PARK DRIVE, ASCENT, #07-13, SINGAPORE 118222
Model Information
Model Name(s)
GRYPHON P PEEK ANCHOR W/DYNACORD GRYPHON P PEEK DS ANCHOR W/DYNACORD
Model Identifier(s)
210122 210123