← Back to catalogue

Mis

FDA UDI

Class II (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name
MIS FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Lance CLEAR pack int. hex. implant Ø5 L13mm, WP FDA UDI
Model / Reference
M5C-13500 FDA UDI
Description
Lance CLEAR pack int. hex. implant Ø5 L13mm, WP FDA UDI

Identifiers

Catalog Number
M5C-13500 FDA UDI
Primary DI / UDI-DI
07290113993181 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Screw endosteal dental implant, two-piece

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

Similar devices

Also classified as Screw 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 61bb8f0e-5974-4e9b-b87f-0c327ff75735 34 fields · synced May 31, 2026