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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 implant system FDA UDI
Device Name
3.25mm Diameter, 4.1mm Platform Straight External Hex Implant Length 8.5mm Sandblast FDA UDI
Model / Reference
T-3SE85S FDA UDI
Description
3.25mm Diameter, 4.1mm Platform Straight External Hex Implant Length 8.5mm Sandblast FDA UDI

Identifiers

Primary DI / UDI-DI
00842448112972 FDA UDI
510(k) Number
K042971 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

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

Category: Dental implant system

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 implant system.

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 f34f9177-6ca9-4ae1-bc0e-18f32ddb3c21 34 fields · synced Jun 8, 2026