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Acteon

FDA UDI

Class II (US FDA UDI)

by Satelec

Identity

Trade Name
ACTEON FDA UDI
Generic Name
Ultrasonic dental scaling/debridement system FDA UDI
Device Name
P5 NEWTRON XS LED: With a self-contained irrigation and LED light, P5 Newtron® XS LED is the full-option generator. It is both equipped with self-contained irrigation and a light handpiece for maximum autonomy, visibility comfort and performance. FDA UDI
Model / Reference
P5 XS LED 115V FDA UDI
Description
P5 NEWTRON XS LED: With a self-contained irrigation and LED light, P5 Newtron® XS LED is the full-option generator. It is both equipped with self-contained irrigation and a light handpiece for maximum autonomy, visibility comfort and performance. FDA UDI

Identifiers

Catalog Number
F58226 FDA UDI
Primary DI / UDI-DI
03609820582269 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Ultrasonic dental scaling/debridement system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultrasonic dental scaling/debridement system

Acteon by Satelec — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic dental scaling/debridement system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Satelec

Sources (1)

  • FDA UDI 993f2ef8-d6d3-46cc-be5c-c16c19a3ef4b 35 fields · synced May 31, 2026