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Ultimate

FDA UDI

Class II (US FDA UDI)

by Spiraltech Superior Dental Implants, Inc.

Identity

Trade Name
Ultimate FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Ultimate Implant Conical 3.5mmx13mm SLA Surface FDA UDI
Model / Reference
ULC35013A FDA UDI
Description
Ultimate Implant Conical 3.5mmx13mm SLA Surface FDA UDI

Identifiers

Catalog Number
ULC35013A FDA UDI
Primary DI / UDI-DI
D890ULC35013A0 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Screw endosteal dental implant, two-piece

Ultimate by Spiraltech Superior Dental Implants, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d93722d8-82dc-471f-82ac-a35fab12da96 35 fields · synced Jun 6, 2026