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Apex® 3000000A1

by Incontrol Medical, LLC

Apex® 3000000A1 is a Class II device made by Incontrol Medical, LLC, cleared under FDA 510(k) K141158 on 26 Nov 2014 and listed in FDA GUDID since 3 Oct 2016 (UDI-DI 00851508007028), 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) K141158

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 Number00851508007028 UDI-DI Date3 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK141158 Date26 Nov 2014DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K141158 decided 26 Nov 2014 Active
  • FDA GUDID UDI-DI 00851508007028 listed 3 Oct 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K141158
  2. Listed FDA GUDID 00851508007028

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Apex®
Generic name
Pelvic floor muscle exerciser
Model / Ref / Catalog
3000000A1
Primary DI / UDI-DI
00851508007028
510(k) Number
FDA product code
KPI
GMDN term
Pelvic floor muscle exerciser
Device class
Class II
Regulation number
876.5320
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 12 Inch

Related devices

Category: Pelvic floor muscle exerciser

Similar devices

Other devices filed under FDA product code KPI (STIMULATOR, ELECTRICAL, NON-IMPLANTABLE, FOR INCONTINENCE).

Other devices from Incontrol Medical, LLC

See all devices from Incontrol Medical, LLC →

Properties

  • Over-the-counter
  • Serial number
Other properties (13, all answered No)