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IPL-Sq

FDA UDI

Class II (US FDA UDI)

by Vydence Medical

Identity

Trade Name
IPL-Sq FDA UDI
Generic Name
Light-energy skin surface treatment system applicator FDA UDI
Device Name
IPL-Sq FDA UDI
Model / Reference
18077 FDA UDI
Description
IPL-Sq FDA UDI

Identifiers

Catalog Number
18077 FDA UDI
Primary DI / UDI-DI
07898961835020 FDA UDI
510(k) Number
K171443 FDA UDI
FDA Product Code
ONF FDA UDI
GMDN Term
Light-energy skin surface treatment system applicator 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Light-energy skin surface treatment system applicator

IPL-Sq by Vydence Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Light-energy skin surface treatment system applicator.

Cleared under the same submission

K171443 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vydence Medical

Sources (1)

  • FDA UDI d1894471-e7b9-4d05-9bf7-29c017e0c605 36 fields · synced Jun 6, 2026