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Iris Acne IPL HP

FDA UDI

Class II (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name
Iris Acne IPL HP FDA UDI
Generic Name
Multi-modality skin surface treatment system FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Catalog Number
AAIP24102205 FDA UDI
Primary DI / UDI-DI
07290110123437 FDA UDI
510(k) Number
K230308 FDA UDI
FDA Product Code
GEX FDA UDI
ILY FDA UDI
ONF FDA UDI
GMDN Term
Multi-modality skin surface treatment system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
890.5500 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

No

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: Multi-modality skin surface treatment system

Iris Acne IPL HP by Alma Lasers Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin surface treatment system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alma Lasers Ltd.

Sources (1)

  • FDA UDI 8f70e63f-13a2-4741-8204-d7b7f6aa2b28 34 fields · synced May 31, 2026