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Arm Support 106024

by Medtec LLC

Arm Support 106024 is a Class II device made by Medtec LLC, cleared under FDA 510(k) K060737 on 31 Mar 2006 and listed in FDA GUDID since 2 Aug 2017 (UDI-DI 00841439100264), 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) K060737

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 Number00841439100264 UDI-DI Date2 Aug 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK060737 Date31 Mar 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K060737 decided 31 Mar 2006 Active
  • FDA GUDID UDI-DI 00841439100264 listed 2 Aug 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K060737
  2. Listed FDA GUDID 00841439100264

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Arm Support
Generic name
Radiological breast positioner, non-wearable
Model / Ref / Catalog
106024
Primary DI / UDI-DI
00841439100264
510(k) Number
FDA product code
IYE
GMDN term
Radiological breast positioner, non-wearable
Device class
Class II
Regulation number
892.5050
GUDID distribution status
In Commercial Distribution
Size
Length — 25.5 Centimeter

Similar devices

Other devices filed under FDA product code IYE (Accelerator, linear, medical).

Other devices from Medtec LLC

See all devices from Medtec LLC →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)