← Back to catalogue

Atlas Implant System

FDA UDI

Class II (US FDA UDI)

by Dentatus AB

Identity

Trade Name
Atlas Implant System FDA UDI
Generic Name
Transgingival implant FDA UDI
Device Name
Dentatus Atlas Implant, blister pack including 1 pc FDA UDI
Model / Reference
AT-22M FDA UDI
Description
Dentatus Atlas Implant, blister pack including 1 pc FDA UDI

Identifiers

Primary DI / UDI-DI
07350081494988 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Transgingival implant 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transgingival implant

Atlas Implant System by Dentatus AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transgingival implant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dentatus AB

Sources (1)

  • FDA UDI 8ce3e9d6-d978-4290-bb96-400bd6acb622 34 fields · synced May 30, 2026