← Back to catalogue

Restoris

FDA UDI

Class II (US FDA UDI)

by MAKO Surgical Corp.

Identity

Trade Name
RESTORIS FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
Femoral Head, CoCr, 12/14 Taper FDA UDI
Model / Reference
186032-03 FDA UDI
Description
Femoral Head, CoCr, 12/14 Taper FDA UDI

Identifiers

Catalog Number
186032-03 FDA UDI
Primary DI / UDI-DI
00848486007898 FDA UDI
510(k) Number
K112802 FDA UDI
FDA Product Code
LPH FDA UDI
OQG FDA UDI
OQH FDA UDI
JDI FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3350 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

Category: Metallic femoral head prosthesis

Restoris by MAKO Surgical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
MAKO Surgical Corp.

Sources (1)

  • FDA UDI 35d7f209-702b-4247-985b-bf1b1aa086ec 36 fields · synced Jun 9, 2026