← Back to catalogue

Mis Provisional Implant

FDA UDI

Class II (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name
MIS PROVISIONAL IMPLANT FDA UDI
Generic Name
Basket endosteal dental implant, two-piece FDA UDI
Device Name
Provisional implant 10mm FDA UDI
Model / Reference
TF1-A1024 FDA UDI
Description
Provisional implant 10mm FDA UDI

Identifiers

Primary DI / UDI-DI
07290108992373 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Basket 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basket endosteal dental implant, two-piece

Mis Provisional Implant by MIS Implants Technologies Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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

Sources (1)

  • FDA UDI 0273e271-9a7c-4801-896c-d1d58cc0f1db 33 fields · synced Jun 1, 2026