Identity
- Trade Name
- The Tether™ FDA UDI
- Generic Name
- Anterior spinal tethering system tether FDA UDI
- Device Name
- Tether Reel Tensioner FDA UDI
- Model / Reference
- 240H6003 FDA UDI
- Description
- Tether Reel Tensioner FDA UDI
Identifiers
- Catalog Number
- 240H6003 FDA UDI
- Primary DI / UDI-DI
- 03662663080835 FDA UDI
- FDA Product Code
- QHP FDA UDI
- GMDN Term
- Anterior spinal tethering system tether FDA UDI
Classification
- Device Class
- N FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Anterior spinal tethering system tether
The Tether™ by Highridge Medical, LLC — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anterior spinal tethering system tether.
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 N | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Highridge Medical, LLC
Sources (1)
- FDA UDI 3c25e120-0bdd-4099-987b-1cc4cca6ac04 35 fields · synced Jun 1, 2026