Skip to content

Bagley REXMR-6LA

by Gyrus Acmi, Inc.

Bagley REXMR-6LA is a Class II device made by Gyrus Acmi, Inc., cleared under FDA 510(k) K052044 on 16 Aug 2005 and listed in FDA GUDID since 24 Jul 2024 (UDI-DI 00821925007833), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K052044

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00821925007833 UDI-DI Date24 Jul 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK052044 Date16 Aug 2005DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K052044 decided 16 Aug 2005 Active
  • FDA GUDID UDI-DI 00821925007833 listed 24 Jul 2024 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K052044
  2. Listed FDA GUDID 00821925007833

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Bagley
Generic name
Rigid optical ureteroscope
Model / reference
REXMR-6LA
Primary DI / UDI-DI
00821925007833
510(k) Number
FDA product code
FGB
GMDN term
Rigid optical ureteroscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid optical ureteroscope

Cleared under the same submission (K052044)

Similar devices in this category

Other devices filed under Rigid optical ureteroscope.

Other devices from Gyrus Acmi, Inc.

See all devices from Gyrus Acmi, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)