Identity
- Trade Name
- MONET FDA UDI
- Generic Name
- General internal orthopaedic fixation system implantation kit FDA UDI
- Device Name
- MODULAR FLEX TIP DRIVER, AO QC FDA UDI
- Model / Reference
- 113.7740 FDA UDI
- Description
- MODULAR FLEX TIP DRIVER, AO QC FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841732129702 FDA UDI
- 510(k) Number
- K182151 FDA UDI
- FDA Product Code
- OVE FDA UDIODP FDA UDI
- GMDN Term
- General internal orthopaedic fixation system implantation kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
Yes
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: General internal orthopaedic fixation system implantation kit
Monet by CTL Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General internal orthopaedic fixation system implantation kit.
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Cleared under the same submission
K182151 also covers:
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
- MONET — CTL Medical Corporation
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- CTL Medical Corporation
Sources (1)
- FDA UDI 12739c47-838f-4b75-a21b-7e98f9255727 35 fields · synced May 31, 2026