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EarClear Rx 90002

by Nuance Medical, LLC

EarClear Rx 90002 is an ear canal irrigation kit (FDA Class I; FDA product code KCP, Syringe, Ent) made by Nuance Medical, LLC, listed in FDA GUDID since 25 Oct 2018 (UDI-DI 00856331006187), 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 Number00856331006187 UDI-DI Date25 Oct 2018ListedStatusListed 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  • Withdrawn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
EarClear Rx
Generic name
Ear canal irrigation kit, reusable
Model / Ref / Catalog
90002
Primary DI / UDI-DI
00856331006187
FDA product code
KCP
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 KCP (SYRINGE, ENT).

Other devices from Nuance Medical, LLC

See all devices from Nuance Medical, LLC →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)