Impression copings

FDA UDI

Class I (US FDA UDI)

by Dentack Implants Ltd

Identity

Trade Name: Impression copings FDA UDI
Generic Name: Screw endosteal dental implant, two-piece FDA UDI
Device Name: Impression copings FDA UDI
Model / Reference: IC-750 FDA UDI
Description: Impression copings FDA UDI

Identifiers

Primary DI / UDI-DI: 07290112280800 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Screw endosteal dental implant, two-piece 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Screw endosteal dental implant, two-piece

Impression copings by Dentack Implants Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dentack Implants Ltd

Sources (1)

FDA UDI fbdb6e01-51e1-4bcf-ac1d-71419ef0bbc5 34 fields · synced May 30, 2026