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Kontact

FDA UDI

Class I (US FDA UDI)

by Biotech Dental

Identity

Trade Name
Kontact FDA UDI
Generic Name
Dental implant abutment analog, laboratory FDA UDI
Device Name
Long scan locator for implant Ø3.0mm +K30VPL screw FDA UDI
Model / Reference
K30PSCANL FDA UDI
Description
Long scan locator for implant Ø3.0mm +K30VPL screw FDA UDI

Identifiers

Primary DI / UDI-DI
03701045274520 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, laboratory 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 implant abutment analog, laboratory

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

Similar devices

Also classified as Dental implant abutment analog, laboratory.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotech Dental

Sources (1)

  • FDA UDI 185cb8b0-3aab-4063-a01e-f0d4d4852c1f 34 fields · synced Jun 8, 2026