← Back to catalogue

Inbone

FDA UDI

Class I (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
INBONE FDA UDI
Generic Name
Orthopaedic implant calibration pin FDA UDI
Device Name
Steinmann Pin FDA UDI
Model / Reference
200072 FDA UDI
Description
Steinmann Pin FDA UDI

Identifiers

Catalog Number
200072 FDA UDI
Primary DI / UDI-DI
00889797058728 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Orthopaedic implant calibration pin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Dimensions & Sizes

Size
Outer Diameter — 2.4 Millimeter FDA UDI
Length — 229 Millimeter FDA UDI

Category: Orthopaedic implant calibration pin

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

Similar devices

Also classified as Orthopaedic implant calibration pin.

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

Sources (1)

  • FDA UDI 861e2b8b-a9ee-4329-9dc5-45951eb4cb5f 36 fields · synced Jun 8, 2026