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Kontact

FDA UDI

Class I (US FDA UDI)

by Biotech Dental

Identity

Trade Name
KONTACT FDA UDI
Generic Name
Dental prosthesis/implant abutment screw analog, reusable FDA UDI
Device Name
Abutment laboratory screw (x5) FDA UDI
Model / Reference
KVPL-5 FDA UDI
Description
Abutment laboratory screw (x5) FDA UDI

Identifiers

Catalog Number
KVPL-5 FDA UDI
Primary DI / UDI-DI
03701045275411 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw analog, reusable 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Dental prosthesis/implant abutment screw analog, reusable

Kontact by Biotech Dental — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis/implant abutment screw analog, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotech Dental

Sources (1)

  • FDA UDI 2cd62cd8-eef2-4ccb-a677-1482d5cbd5e3 35 fields · synced Jun 1, 2026