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C&B Prosthetic Kit

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name
C&B PROSTHETIC KIT FDA UDI
Generic Name
Dental prosthesis/implant abutment screw analog, single-use FDA UDI
Device Name
5.0MM ISI CROWN & BRIDGE PROSTHETIC KIT FDA UDI
Model / Reference
5.0MM ISI C & B PROSTHETIC KIT FDA UDI
Description
5.0MM ISI CROWN & BRIDGE PROSTHETIC KIT FDA UDI

Identifiers

Catalog Number
5.0 I-CB PK (F) FDA UDI
Primary DI / UDI-DI
D78550ICBPKF0 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw analog, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
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

Yes

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

Category: Dental implant analogDental prosthesis/implant abutment screw analog, single-use

C&B Prosthetic Kit by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis/implant abutment screw analog, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oco Biomedical

Sources (1)

  • FDA UDI 3962983c-c143-4b4c-8ebd-751fe995feb2 34 fields · synced Jun 6, 2026