← Back to catalogue

Cover Screw

FDA UDI

Class II (US FDA UDI)

by Dentack Implants Ltd

Identity

Trade Name
Cover Screw FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Cover Screw FDA UDI
Model / Reference
377701 FDA UDI
Description
Cover Screw FDA UDI

Identifiers

Primary DI / UDI-DI
07290112280503 FDA UDI
510(k) Number
K152188 FDA UDI
FDA Product Code
NHA FDA UDI
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Screw endosteal dental implant, two-piece

Cover Screw by Dentack Implants Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw endosteal dental implant, two-piece.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 945c0683-9c52-4a74-96ce-45c109ad936c 35 fields · synced May 30, 2026