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Simplant

FDA UDI

Class I (US FDA UDI)

by Dentsply Implants Manufacturing GmbH

Identity

Trade Name
SIMPLANT FDA UDI
Generic Name
Dental implantation drilling template, custom-made FDA UDI
Device Name
Guide File DS design FDA UDI
Model / Reference
37472 FDA UDI
Description
Guide File DS design FDA UDI

Identifiers

Catalog Number
37472 FDA UDI
Primary DI / UDI-DI
07392532290459 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation drilling template, custom-made 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

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 implantation drilling template, custom-made

Simplant by Dentsply Implants Manufacturing GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation drilling template, custom-made.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI caca6b15-4953-4b62-b0d7-3e6a52365dbd 34 fields · synced Jun 8, 2026