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MultiLite Dye Handpiece Kir

FDA UDI

Class I (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
MultiLite Dye Handpiece Kir FDA UDI
Generic Name
Dermatological frequency-doubled solid-state laser system FDA UDI
Device Name
C6 Dye Handpiece Kit FDA UDI
Model / Reference
100-7017-067 FDA UDI
Description
C6 Dye Handpiece Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00841494103637 FDA UDI
510(k) Number
K014234 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Dermatological frequency-doubled solid-state laser system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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

No

FDA UDI

Category: Dermatological frequency-doubled solid-state laser system

MultiLite Dye Handpiece Kir by Cynosure, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological frequency-doubled solid-state laser system.

Cleared under the same submission

K014234 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI 612b51a8-0f13-43f7-ad5b-b0713cf0dc17 34 fields · synced May 30, 2026