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Jedmed 30-1835

by JEDMED Instrument Company

Jedmed 30-1835 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 1 Sep 2020 (UDI-DI M6333018350), 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 NumberM6333018350 UDI-DI Date1 Sep 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Jedmed
Generic name
Middle ear incus hook
Model / Ref / Catalog
30-1835
Primary DI / UDI-DI
M6333018350
FDA product code
JYL
GMDN term
Middle ear incus hook
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Incus hook

Similar devices

Other devices filed under FDA product code JYL (Hook, Microsurgical Ear).

Other devices from JEDMED Instrument Company

See all devices from JEDMED Instrument Company →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)