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HR 690XL Light Block package

FDA UDI

Class II (US FDA UDI)

by Venus Concept Inc.

Identity

Trade Name
HR 690XL Light Block package FDA UDI
Generic Name
Multi-modality skin surface treatment system FDA UDI
Model / Reference
PK000324 FDA UDI

Identifiers

Primary DI / UDI-DI
27290016541179 FDA UDI
510(k) Number
K153717 FDA UDI
FDA Product Code
GEX 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
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

No

FDA UDI

Category: Multi-modality skin surface treatment system

HR 690XL Light Block package by Venus Concept Inc. — 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
Venus Concept Inc.

Sources (1)

  • FDA UDI b2215d82-56b2-4678-830b-63f5f28dc998 33 fields · synced May 30, 2026