Identity
- Trade Name
- HEALIX ADVANCE DYNATAPE DYNACORD FDA UDI
- Generic Name
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
- Device Name
- HEALIX ADVANCE BR Anchor w/ DYNATAPE Suture TCP/PLGA Absorbable Anchor with (1) 2.5mm Black/Blue DYNATAPE Braided Flat Suture, 36inch (91 cm) and (1) White/Blue/Green, Size 2 (5 metric) DYNACORD Braided Suture, 36inch (91cm), (1) Utility Shuttle Suture BLACK 6.5mm FDA UDI
- Model / Reference
- 280737 FDA UDI
- Description
- HEALIX ADVANCE BR Anchor w/ DYNATAPE Suture TCP/PLGA Absorbable Anchor with (1) 2.5mm Black/Blue DYNATAPE Braided Flat Suture, 36inch (91 cm) and (1) White/Blue/Green, Size 2 (5 metric) DYNACORD Braided Suture, 36inch (91cm), (1) Utility Shuttle Suture BLACK 6.5mm FDA UDI
Identifiers
- Catalog Number
- 280737 FDA UDI
- Primary DI / UDI-DI
- 10886705031085 FDA UDI
- 510(k) Number
- K200949 FDA UDI
- FDA Product Code
- MAI FDA UDI
- GMDN Term
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Tendon/ligament bone anchor, bioabsorbable
Healix Advance Dynatape Dynacord by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tendon/ligament bone anchor, bioabsorbable.
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- 5 x 15mm CitreLock Implant — ACUITIVE TECHNOLOGIES · Class II
- Fix2Lock — OSTEONIC CO., Ltd. · Class II
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Twist — PARCUS MEDICAL LLC · Class II
Cleared under the same submission
K200949 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI f5fecf91-ac24-44c2-b053-c799a7969d82 37 fields · synced May 31, 2026