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Coriograph

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
CORIOGRAPH FDA UDI
Generic Name
Orthopaedic/craniofacial implantation planning software FDA UDI
Device Name
CORIOGRAPH Shoulder Pre-Operative Planning and Modeling Services V1.0. Modules in scope: CORIOGRAPH Shoulder Pre-Op Plan CORIOGRAPH Modeler for Shoulder FDA UDI
Model / Reference
ROB20033 FDA UDI
Description
CORIOGRAPH Shoulder Pre-Operative Planning and Modeling Services V1.0. Modules in scope: CORIOGRAPH Shoulder Pre-Op Plan CORIOGRAPH Modeler for Shoulder FDA UDI

Identifiers

Catalog Number
ROB20033 FDA UDI
Primary DI / UDI-DI
00885556924761 FDA UDI
510(k) Number
K250921 FDA UDI
FDA Product Code
PBF FDA UDI
GMDN Term
Orthopaedic/craniofacial implantation planning software 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic/craniofacial implantation planning software

Coriograph by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic/craniofacial implantation planning software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 7cb0ff48-26d7-4216-9b8b-159eb85fcd7a 36 fields · synced Jun 8, 2026