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Flex 24324

by Medrobotics Corporation

Flex 24324 is a Class II device made by Medrobotics Corporation, cleared under FDA 510(k) K150776 on 17 Jul 2015 and listed in FDA GUDID since 7 Dec 2018 (UDI-DI 00850190004049), active as of 22 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 22 Oct 2026

Documents

510(k) K150776

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850190004049 UDI-DI Date7 Dec 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK150776 Date17 Jul 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K150776 decided 17 Jul 2015 Active
  • FDA GUDID UDI-DI 00850190004049 listed 7 Dec 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K150776
  2. Listed FDA GUDID 00850190004049

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Flex
Generic name
Flexible video otorhinolaryngoscope, reusable
Model / reference
24324
Primary DI / UDI-DI
00850190004049
510(k) Number
FDA product code
EOB
GMDN term
Flexible video otorhinolaryngoscope, reusable
Device class
Class II
Regulation number
874.4760
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible video otorhinolaryngoscope, reusable

Cleared under the same submission (K150776)

and 8 more cleared under K150776

Similar devices

Other devices filed under FDA product code EOB (Nasopharyngoscope (Flexible Or Rigid)).

Other devices from Medrobotics Corporation

  • Flex 25386

    Class II

  • Flex 24324-L

    Class II

  • Flex 50124PKG

    Class I

  • Flex 50208PKG

    Class I

See all devices from Medrobotics Corporation →

Properties

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