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OnPoint Lite System

FDA UDI

Class II (US FDA UDI)

by Biovision Technologies, Llc

Identity

Trade Name
OnPoint Lite System FDA UDI
Generic Name
Endoscopic video imaging system FDA UDI
Device Name
OnPoint Lite Visualization System FDA UDI
Model / Reference
24-4200 FDA UDI
Description
OnPoint Lite Visualization System FDA UDI

Identifiers

Catalog Number
BMT01197-00001 FDA UDI
Primary DI / UDI-DI
00851582006108 FDA UDI
510(k) Number
K143705 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic video imaging system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopic video imaging system

OnPoint Lite System by Biovision Technologies, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video imaging system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a7e2283-1a3c-4cb6-8986-5ee43ff05efa 36 fields · synced Jun 8, 2026