Identity
- Trade Name
- RESTORIS FDA UDI
- Generic Name
- Surgical instrument handle, non-torque-limiting FDA UDI
- Device Name
- TIBIAL ONLAY ONLAY HANDLE FDA UDI
- Model / Reference
- 120137 FDA UDI
- Description
- TIBIAL ONLAY ONLAY HANDLE FDA UDI
Identifiers
- Catalog Number
- 120137 FDA UDI
- Primary DI / UDI-DI
- 00848486018108 FDA UDI
- FDA Product Code
- NPJ FDA UDIHSX FDA UDIKRR FDA UDIHRY FDA UDI
- GMDN Term
- Surgical instrument handle, non-torque-limiting FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 FDA UDI888.3520 FDA UDI888.3540 FDA UDI888.3530 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
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
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical instrument handle, non-torque-limiting
Restoris by MAKO Surgical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical instrument handle, non-torque-limiting.
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Cleared under the same submission
K082172 also covers:
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
K090763 also covers:
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
- RESTORIS — MAKO Surgical Corp.
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
- MAKO Surgical Corp.
Sources (1)
- FDA UDI e88cc232-a1b9-45b8-8f1b-e1e4f26b26db 35 fields · synced Jun 9, 2026