Skip to content

Acteon P5 Xs LED 115V No Tips

by Satelec

Acteon P5 Xs LED 115V No Tips (F58230) is a Class II device made by Satelec, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 03609820582306), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03609820582306 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Acteon
Generic name
Ultrasonic dental scaling/debridement system
Model / Ref / Catalog
P5 XS LED 115V NO TIPS, F58230
Primary DI / UDI-DI
03609820582306
FDA product code
ELC
GMDN term
Ultrasonic dental scaling/debridement system
Device class
Class II
Regulation number
872.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ultrasonic dental scaling/debridement system

Similar devices in this category

Other devices filed under Ultrasonic dental scaling/debridement system.

Other devices from Satelec

See all devices from Satelec →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)