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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
C1 XD coni. con. implant D5 L13mm , WP FDA UDI
Model / Reference
C1-D13500 FDA UDI
Description
C1 XD coni. con. implant D5 L13mm , WP FDA UDI

Identifiers

Catalog Number
C1-D13500 FDA UDI
Primary DI / UDI-DI
07290113996205 FDA UDI
510(k) Number
K112162 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 990ed476-af15-403b-8f01-d19ff42d7df2 35 fields · synced May 30, 2026