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EndoraGard 29520DX

by Kerr Corporation

EndoraGard 29520DX is a Class I device made by Kerr Corporation, listed in FDA GUDID since 31 Aug 2017 (UDI-DI 00615375001721), 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 Number00615375001721 UDI-DI Date31 Aug 2017ListedStatusListed 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  • Withdrawn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
EndoraGard
Generic name
Intubation teeth protector
Model / reference
29520DX
Primary DI / UDI-DI
00615375001721
FDA product code
BRW
GMDN term
Intubation teeth protector
Device class
Class I
Regulation number
868.5820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intubation teeth protector

Similar devices

Other devices filed under FDA product code BRW (PROTECTOR, DENTAL).

Other devices from Kerr Corporation

See all devices from Kerr Corporation →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)