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Titan Implants Inc

FDA UDI

Class II (US FDA UDI)

by Titan Implant Inc

Identity

Trade Name
TITAN IMPLANTS INC FDA UDI
Generic Name
Dental prosthesis/implant abutment screw FDA UDI
Device Name
4.1mm External Hex Multi-Unit Abutment Sleeve Screw GH 3mm FDA UDI
Model / Reference
NB-MCASS-3.0 FDA UDI
Description
4.1mm External Hex Multi-Unit Abutment Sleeve Screw GH 3mm FDA UDI

Identifiers

Primary DI / UDI-DI
00842448116543 FDA UDI
510(k) Number
K042971 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw FDA UDI

Classification

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

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental prosthesis/implant abutment screw

Titan Implants Inc by Titan Implant Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis/implant abutment screw.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Titan Implant Inc

Sources (1)

  • FDA UDI ad6233ee-dcd8-4abd-bcf2-e948071d639e 34 fields · synced Jun 1, 2026