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Acteon

FDA UDI

Class II (US FDA UDI)

by Satelec

Identity

Trade Name
ACTEON FDA UDI
Generic Name
Dental ultrasonic surgical system FDA UDI
Device Name
With Piezotome® 2, take full advantage of ACTEON®’s ultrasonic expertise in dental as well as in surgical piezoelectric treatments. FDA UDI
Model / Reference
PIEZOTOME 2 GP FDA UDI
Description
With Piezotome® 2, take full advantage of ACTEON®’s ultrasonic expertise in dental as well as in surgical piezoelectric treatments. FDA UDI

Identifiers

Catalog Number
F57415 FDA UDI
Primary DI / UDI-DI
03609820574158 FDA UDI
510(k) Number
K091331 FDA UDI
FDA Product Code
DZI FDA UDI
GMDN Term
Dental ultrasonic surgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental ultrasonic surgical system

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

Similar devices

Also classified as Dental ultrasonic surgical system.

Cleared under the same submission

K091331 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Satelec

Sources (1)

  • FDA UDI bc81546d-ba2a-47e1-b738-a16b842837fa 36 fields · synced May 30, 2026