← Back to catalogue

Acrylic Coping

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name
ACRYLIC COPING FDA UDI
Generic Name
Dental implant abutment impression cap FDA UDI
Device Name
5.0mm ACRYLIC COPING FOR ISI/TSI CROWN AND BRIDGE FDA UDI
Model / Reference
5.0mm ACRYLIC COPING FOR ISI/TSI C&B FDA UDI
Description
5.0mm ACRYLIC COPING FOR ISI/TSI CROWN AND BRIDGE FDA UDI

Identifiers

Catalog Number
5.0 AC FDA UDI
Primary DI / UDI-DI
D78550AC0 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment impression cap 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

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

Category: Dental implant abutment impression cap

Acrylic Coping by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant abutment impression cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Oco Biomedical

Sources (1)

  • FDA UDI 1ac335ae-e8c6-4483-b6d8-276c0f3a80e6 34 fields · synced May 30, 2026