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Elevator

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
ELEVATOR FDA UDI
Generic Name
Dental elevator, sinus lift FDA UDI
Device Name
SINUS LIFT, CLARIZIO, DOUBLE ENDED, NARROW FDA UDI
Model / Reference
01-105-96-07 FDA UDI
Description
SINUS LIFT, CLARIZIO, DOUBLE ENDED, NARROW FDA UDI

Identifiers

Primary DI / UDI-DI
00888118005113 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Dental elevator, sinus lift FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental elevator, sinus lift

Elevator by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental elevator, sinus lift.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI c3495af6-391e-4d2a-95d6-ecec1652e47e 35 fields · synced Jun 8, 2026