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Enova Illumination

FDA UDI

Class I (US FDA UDI)

by Enova Illumination, Inc

Identity

Trade Name
Enova Illumination FDA UDI
Generic Name
Surgical binoculars, reusable FDA UDI
Device Name
Vizix Prismatic 5.5x Oculars FDA UDI
Model / Reference
820007-001 FDA UDI
Description
Vizix Prismatic 5.5x Oculars FDA UDI

Identifiers

Primary DI / UDI-DI
00810186670108 FDA UDI
FDA Product Code
FSP FDA UDI
GMDN Term
Surgical binoculars, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical binoculars, reusable

Enova Illumination by Enova Illumination, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical binoculars, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3bab4586-c486-4202-84b0-170f4cb3d18c 33 fields · synced May 30, 2026