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restor3d Utility Wedge

FDA UDI

Class II (US FDA UDI)

by Restor3D

Identity

Trade Name
restor3d Utility Wedge FDA UDI
Generic Name
Metallic osteotomy fusion cage, non-customized FDA UDI
Device Name
Titanium (Ti-6AI-4V) Subtalar Wedge, Right foot, Small Footprint, 12mm Thickness, 5 Degree FDA UDI
Model / Reference
1105-2719120505R FDA UDI
Description
Titanium (Ti-6AI-4V) Subtalar Wedge, Right foot, Small Footprint, 12mm Thickness, 5 Degree FDA UDI

Identifiers

Primary DI / UDI-DI
00840097503370 FDA UDI
510(k) Number
K201314 FDA UDI
FDA Product Code
PLF FDA UDI
GMDN Term
Metallic osteotomy fusion cage, non-customized FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Metallic osteotomy fusion cage, non-customized

restor3d Utility Wedge by Restor3D — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic osteotomy fusion cage, non-customized.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Restor3D

Sources (1)

  • FDA UDI 04f518bf-b489-480e-bb37-76cab2c3f329 34 fields · synced Jun 8, 2026