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Ortholoc 3di

FDA UDI

Class I (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
ORTHOLOC 3DI FDA UDI
Generic Name
Bone approximation clamp FDA UDI
Device Name
Small Bones FDA UDI
Model / Reference
52030617 FDA UDI
Description
Small Bones FDA UDI

Identifiers

Catalog Number
52030617 FDA UDI
Primary DI / UDI-DI
00840420185600 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Bone approximation clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone approximation clamp

Ortholoc 3di by Wright Medical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone approximation clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab75dc47-1fe3-416a-a43b-4f4b5ae9a0f7 35 fields · synced Jun 6, 2026