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Jenx STZ02-C2-04

by Jenx Limited

Jenx STZ02-C2-04 is a Class I device made by Jenx Limited, listed in FDA GUDID since 13 Feb 2024 (UDI-DI 05056235222651), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05056235222651 UDI-DI Date13 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  • Withdrawn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
Jenx
Generic name
Manual stander
Model / reference
STZ02-C2-04
Primary DI / UDI-DI
05056235222651
FDA product code
INW
GMDN term
Manual stander
Device class
Class I
Regulation number
890.3750
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual stander

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Other devices from Jenx Limited

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)