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Brevis

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 260-300-434

by Bicon, LLC

Identity

Trade Name
Brevis EUDAMEDFDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Dental Abutment EUDAMED
2.0mm 0° Brevis™ Abutment - 3.0mm Post FDA UDI
Model / Reference
260-300-434 EUDAMEDFDA UDI
Description
2.0mm 0° Brevis™ Abutment - 3.0mm Post FDA UDI

Identifiers

Catalog Number
260-300-434 FDA UDI
Primary DI / UDI-DI
00813110022325 EUDAMEDFDA UDI
Basic UDI-DI
B-00813110022325 EUDAMED
081311002TAbut5L EUDAMED
510(k) Number
K853788 FDA UDI
FDA Product Code
DZE FDA UDI
EMDN Code
P010299 ODONTOLOGICAL PROSTHESES - OTHER EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Brevis by Bicon, Llc — Class IIb — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bicon, LLC
EUDAMED SRN
US-MF-000002782
Authorised Representative
Bicon Europe Ltd IE-AR-000002497

Sources (3)

  • EUDAMED b9b63308-081b-4b0e-b66e-434215bdfbbf 61 fields · synced Jun 8, 2026
  • EUDAMED d8ae73a0-25cc-4dfe-b6f0-673cc3288b4b 61 fields · synced May 19, 2026
  • FDA UDI d781165e-368e-40dd-8ee4-cf2630f4c2e6 36 fields · synced May 30, 2026