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ProStim Electrodes 31700

by AliMed, LLC 7 variants

ProStim Electrodes 31700 (31705) is a Class II device made by AliMed, LLC, cleared under FDA 510(k) K130987 on 17 Jul 2013 and listed in FDA GUDID since 1 Sep 2016 (UDI-DI 00733657258387), 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) K130987

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 Number00733657258387 UDI-DI Date1 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK130987 Date17 Jul 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K130987 decided 17 Jul 2013 Active
  • FDA GUDID UDI-DI 00733657258387 listed 1 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K130987
  2. Listed FDA GUDID 00733657258387

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
ProStim Electrodes
Generic name
Transcutaneous electrical stimulation electrode, single-use
Model / Ref / Catalog
31700, 31705
Primary DI / UDI-DI
00733657258387
510(k) Number
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 2 Inch

Similar devices

Other devices filed under FDA product code GXY (ELECTRODE, CUTANEOUS).

Other devices from AliMed, LLC

See all devices from AliMed, LLC →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)