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Polylase

FDA UDI

Class II (US FDA UDI)

by Ddc Technologies, Inc.

Identity

Trade Name
Polylase FDA UDI
Generic Name
Dermatological solid-state laser system FDA UDI
Device Name
Dual Output Pulsed Alexandrite and Nd:YAG Laser FDA UDI
Model / Reference
MX FDA UDI
Description
Dual Output Pulsed Alexandrite and Nd:YAG Laser FDA UDI

Identifiers

Catalog Number
Polylase MX FDA UDI
Primary DI / UDI-DI
00860002307046 FDA UDI
510(k) Number
K040055 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dermatological solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermatological solid-state laser system

Polylase by Ddc Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological solid-state laser system.

Cleared under the same submission

K040055 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4274030e-adc3-4bac-9ced-f9c4172dc4b9 36 fields · synced May 29, 2026