Skip to content

Curaplex 2115-01975

by Bound Tree Medical, LLC

Curaplex 2115-01975 is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 14 Dec 2016 (UDI-DI 00815277020497), 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 Number00815277020497 UDI-DI Date14 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  • Withdrawn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
Basic endotracheal tube, single-use
Model / Ref / Catalog
2115-01975
Primary DI / UDI-DI
00815277020497
FDA product code
FMF, LNZ
GMDN term
Basic endotracheal tube, single-use
Device class
Class II
Regulation number
880.5860, 868.5730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic endotracheal tube, single-useGeneral-purpose syringe, single-useArtificial airway stylet, single-useEndotracheal tube holder

Similar devices in this category

Other devices filed under Endotracheal tube holder.

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)