Jenx JM20

by Jenx Limited

Jenx JM20 is a Class I device made by Jenx Limited, listed in FDA GUDID since 29 Sep 2023 (UDI-DI 05056235205692), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05056235205692 UDI-DI	Date29 Sep 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 05056235205692

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Jenx
Generic name: Wheelchair/chair/stander occupant restraint/support
Model / reference: JM20

Primary DI / UDI-DI: 05056235205692
FDA product code: INN
GMDN term: Wheelchair/chair/stander occupant restraint/support

Device class: Class I
Regulation number: 890.3100
GUDID distribution status: In Commercial Distribution

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Properties

Premarket exempt
Lot / batch number
Manufacturing date

Other properties (12, all answered No)