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Curaplex 590500K

by Bound Tree Medical, LLC

Curaplex 590500K is an emergency airway clearance suction system (FDA Class II; FDA product code BTA, Pump, Portable, Aspiration (Manual or Powered)) made by Bound Tree Medical, LLC, listed in FDA GUDID since 16 Dec 2016 (UDI-DI 00815277021159), 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 Number00815277021159 UDI-DI Date16 Dec 2016ListedStatusListed 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  • Withdrawn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
Emergency airway clearance suction system, electric
Model / reference
590500K
Description
QUICKDRAW DEPLOY KIT
Primary DI / UDI-DI
00815277021159
FDA product code
BTA
GMDN term
Emergency airway clearance suction system, electric
Device class
Class II
Regulation number
878.4780
GUDID distribution status
In Commercial Distribution

Related devices

Category: Emergency airway clearance suction system, electric

Similar devices

Other devices filed under FDA product code BTA (PUMP, PORTABLE, ASPIRATION (MANUAL OR POWERED)).

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
Other properties (10, all answered No)