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Liposat Pro plus 00003974

by Möller Medical GmbH

Liposat Pro plus 00003974 is a Class II device made by Möller Medical GmbH, cleared under FDA 510(k) K053451 on 25 Aug 2006 and listed in FDA GUDID since 21 Jan 2020 (UDI-DI 04260632792308), 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) K053451

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 Number04260632792308 UDI-DI Date21 Jan 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK053451 Date25 Aug 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K053451 decided 25 Aug 2006 Active
  • FDA GUDID UDI-DI 04260632792308 listed 21 Jan 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K053451
  2. Listed FDA GUDID 04260632792308

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Liposat Pro plus
Generic name
Liposuction system
Model / reference
00003974
Primary DI / UDI-DI
04260632792308
510(k) Number
FDA product code
MUU
GMDN term
Liposuction system
Device class
Class II
Regulation number
878.5040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Liposuction system

Cleared under the same submission (K053451)

and 4 more cleared under K053451

Similar devices in this category

Other devices filed under Liposuction system.

Other devices from Möller Medical GmbH

See all devices from Möller Medical GmbH →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)