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MULTIflex LUX Coupling 465 LRN

FDA UDI

Class I (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name
MULTIflex LUX Coupling 465 LRN FDA UDI
Generic Name
Dental surgical power tool motor, pneumatic FDA UDI
Model / Reference
0.553.1550 FDA UDI

Identifiers

Catalog Number
465 LRN FDA UDI
Primary DI / UDI-DI
EKAV055315500 FDA UDI
510(k) Number
K073478 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental surgical power tool motor, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motor, pneumatic

MULTIflex LUX Coupling 465 LRN by KaVo Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motor, pneumatic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KaVo Dental GmbH

Sources (1)

  • FDA UDI 48e7cd40-b174-4118-b107-37c37b7a24ec 36 fields · synced Jun 8, 2026