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Vision Led

FDA UDI

Class II (US FDA UDI)

by Avante

Identity

Trade Name
VISION LED FDA UDI
Generic Name
Medical monitor/light mount FDA UDI
Device Name
DRE Vision LED, FLOOR MODEL, BATTERY BACKUP FDA UDI
Model / Reference
DRE 061523B FDA UDI
Description
DRE Vision LED, FLOOR MODEL, BATTERY BACKUP FDA UDI

Identifiers

Primary DI / UDI-DI
00815871022422 FDA UDI
510(k) Number
K100388 FDA UDI
FDA Product Code
FST FDA UDI
GMDN Term
Medical monitor/light mount FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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: Medical monitor/light mount

Vision Led by Avante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical monitor/light mount.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avante

Sources (1)

  • FDA UDI b900a0de-90d4-44df-bf1a-6453442370fd 34 fields · synced May 30, 2026