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Model

FDA UDI

Class I (US FDA UDI)

by Bicon, Llc

Identity

Trade Name
Model FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Crown Model FDA UDI
Model / Reference
260-102-115 FDA UDI
Description
Crown Model FDA UDI

Identifiers

Catalog Number
260-102-115 FDA UDI
Primary DI / UDI-DI
00813110024626 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed 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

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Model by Bicon, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bicon, Llc

Sources (1)

  • FDA UDI fb6d0595-727c-414f-a5fc-8a7fe5b8ea76 35 fields · synced Jun 1, 2026