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Implant-One

FDA UDI

Class I (US FDA UDI)

by Implant Logistics, Inc.

Identity

Trade Name
Implant-One FDA UDI
Generic Name
Dental implantation drilling template guide-sleeve FDA UDI
Device Name
4.5mm Drill Guide Sleeve FDA UDI
Model / Reference
3DDX-4.5 FDA UDI
Description
4.5mm Drill Guide Sleeve FDA UDI

Identifiers

Primary DI / UDI-DI
D7623DDX450 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation drilling template guide-sleeve 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

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 implantation drilling template guide-sleeve

Implant-One by Implant Logistics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation drilling template guide-sleeve.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc0e2e94-61fb-497f-b08f-1c156737c846 34 fields · synced Jun 7, 2026