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Penumbra System PMX110

by Penumbra, Inc.

Penumbra System PMX110 is a Class II device made by Penumbra, Inc., cleared under FDA 510(k) K122756 on 2 Oct 2012 and listed in FDA GUDID since 30 Jul 2016 (UDI-DI 00814548012773), 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) K122756

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 Number00814548012773 UDI-DI Date30 Jul 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK122756 Date2 Oct 2012DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K122756 decided 2 Oct 2012 Active
  • FDA GUDID UDI-DI 00814548012773 listed 30 Jul 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K122756
  2. Listed FDA GUDID 00814548012773

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Penumbra System
Generic name
Surgical irrigation/aspiration system
Model / reference
PMX110
Primary DI / UDI-DI
00814548012773
510(k) Number
FDA product code
JCX
GMDN term
Surgical irrigation/aspiration system
Device class
Class II
Regulation number
878.4780
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JCX (APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED).

Other devices from Penumbra, Inc.

See all devices from Penumbra, Inc. →

Properties

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