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Geo Scanbody

FDA UDI

Class I (US FDA UDI)

by Geomedi Inc.

Identity

Trade Name
Geo Scanbody FDA UDI
Generic Name
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI
Device Name
Geo Scanbody is a dental implant surgical instrument used for digital impression acquisition to create an oral reproduction model after implant fixture placement. It has a cross-sectional shape for directional and positional indication, and is connected to the fixture by a screw-retained method. FDA UDI
Model / Reference
SC-MMN FDA UDI
Description
Geo Scanbody is a dental implant surgical instrument used for digital impression acquisition to create an oral reproduction model after implant fixture placement. It has a cross-sectional shape for directional and positional indication, and is connected to the fixture by a screw-retained method. FDA UDI

Identifiers

Primary DI / UDI-DI
08800028710958 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, intraoral-scanning, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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
MRI Safety
MR Conditional FDA UDI

Geo Scanbody by Geomedi Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Geomedi Inc.

Sources (1)

  • FDA UDI f3125c62-b547-4069-acdf-30c214684639 34 fields · synced May 30, 2026