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Plason SLM-9600

by SeoulinMedicare Co., Ltd.

Plason SLM-9600 is a hand-held electric massager (FDA Class I; FDA product code ISA, Massager, Therapeutic, Electric) made by SeoulinMedicare Co., Ltd., listed in FDA GUDID since 27 May 2022 (UDI-DI 08800066190026), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800066190026 UDI-DI Date27 May 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Plason
Generic name
Hand-held electric massager
Model / reference
SLM-9600
Primary DI / UDI-DI
08800066190026
FDA product code
ISA
GMDN term
Hand-held electric massager
Device class
Class I
Regulation number
890.5660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hand-held electric massager

Other devices from SeoulinMedicare Co., Ltd.

See all devices from SeoulinMedicare Co., Ltd. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)