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Curaplex SEENEBK

by Bound Tree Medical, LLC

Curaplex SEENEBK is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 31 Jan 2019 (UDI-DI 00812277033632), 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 Number00812277033632 UDI-DI Date31 Jan 2019ListedStatusListed 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  • Withdrawn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
Curaplex
Generic name
Nebulizing system delivery set, single-use
Model / Ref / Catalog
SEENEBK
Primary DI / UDI-DI
00812277033632
FDA product code
CAF
GMDN term
Nebulizing system delivery set, single-use
Device class
Class II
Regulation number
868.5630
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nebulizing system delivery set, single-use

Similar devices

Other devices filed under FDA product code CAF (NEBULIZER (DIRECT PATIENT INTERFACE)).

Other devices from Bound Tree Medical, LLC

See all devices from Bound Tree Medical, LLC →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)