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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 handpiece tip FDA UDI
Device Name
Spatula used for Schneider membrane elevation Inside the sinus and for desengagement of anatomical structures FDA UDI
Model / Reference
TIP SL5 FDA UDI
Description
Spatula used for Schneider membrane elevation Inside the sinus and for desengagement of anatomical structures FDA UDI

Identifiers

Catalog Number
F87315 FDA UDI
Primary DI / UDI-DI
03609820873152 FDA UDI
510(k) Number
K091252 FDA UDI
FDA Product Code
DZI FDA UDI
GMDN Term
Dental ultrasonic surgical system handpiece tip 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental ultrasonic surgical system handpiece tip

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

Similar devices

Also classified as Dental ultrasonic surgical system handpiece tip.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Satelec

Sources (1)

  • FDA UDI 50869049-8c35-423e-b0f3-acedf2b2718c 36 fields · synced May 31, 2026