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VisionOne V1.0.0

by PeriVision SA

VisionOne V1.0.0 is a Class I device made by PeriVision SA, listed in FDA GUDID since 28 Feb 2024 (UDI-DI 07649990085036), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07649990085036 UDI-DI Date28 Feb 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
VisionOne
Generic name
Perimeter, automatic
Model / reference
V1.0.0
Primary DI / UDI-DI
07649990085036
FDA product code
HPT
GMDN term
Perimeter, automatic
Device class
Class I
Regulation number
886.1605
GUDID distribution status
In Commercial Distribution

Related devices

Category: Perimeter, automatic

Similar devices in this category

Other devices filed under Perimeter, automatic.

Other devices from PeriVision SA

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)