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Mis Seven

FDA UDI

Class II (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name
MIS SEVEN FDA UDI
Generic Name
Basket endosteal dental implant, two-piece FDA UDI
Device Name
Seven internal hex. implant dia. 3.30 L 11.50mm NP FDA UDI
Model / Reference
MF7-11330 FDA UDI
Description
Seven internal hex. implant dia. 3.30 L 11.50mm NP FDA UDI

Identifiers

Primary DI / UDI-DI
07290108999570 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 Seven 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

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Manufacturer

Sources (1)

  • FDA UDI ffed4795-0b5c-43d7-852d-6ca2608fde93 33 fields · synced May 30, 2026