Identity
- Trade Name
- Mako FDA UDI
- Generic Name
- Unicondylar knee prosthesis FDA UDI
- Device Name
- MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 10 MM FDA UDI
- Model / Reference
- 180737-3-E FDA UDI
- Description
- MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 7 - 10 MM FDA UDI
Identifiers
- Catalog Number
- 180737-3-E FDA UDI
- Primary DI / UDI-DI
- 07613327386196 FDA UDI
- FDA Product Code
- HSX FDA UDI
- GMDN Term
- Unicondylar knee prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3520 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Unicondylar knee prosthesis
Mako by MAKO Surgical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Unicondylar knee prosthesis.
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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
- MAKO Surgical Corp.
Sources (1)
- FDA UDI c5c675af-f17f-4099-8a85-f1a7dcfee3d7 35 fields · synced Jun 9, 2026