Skip to content

Ear Wax Removal Kit 702

by Bionix, LLC

Ear Wax Removal Kit 702 is an ear canal irrigation kit (FDA Class I; FDA product code LRD, Applicator, Ent Drug) made by Bionix, LLC, listed in FDA GUDID since 11 Jul 2024 (UDI-DI 00714646000675), 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 Number00714646000675 UDI-DI Date11 Jul 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  • Withdrawn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
Ear Wax Removal Kit
Generic name
Ear canal irrigation kit, reusable
Model / Ref / Catalog
702
Primary DI / UDI-DI
00714646000675
FDA product code
LRD
GMDN term
Ear canal irrigation kit, reusable
Device class
Class I
Regulation number
874.5220
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ear canal irrigation kit, reusable

Similar devices

Other devices filed under FDA product code LRD (APPLICATOR, ENT DRUG).

Other devices from Bionix, LLC

See all devices from Bionix, LLC →

Properties

  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)