EndoActivator

FDA UDI

Class I (US FDA UDI)

by Tulsa Dental Products Llc

Identity

Trade Name: EndoActivator FDA UDI
Generic Name: Ultrasonic dental scaling/debridement system FDA UDI
Device Name: Endo Activator System Kit FDA UDI
Model / Reference: EAS100 FDA UDI
Description: Endo Activator System Kit FDA UDI

Identifiers

Catalog Number: EAS100 FDA UDI
Primary DI / UDI-DI: D716EAS1001 FDA UDI
FDA Product Code: JET FDA UDI
GMDN Term: Ultrasonic dental scaling/debridement system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6650 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Liquid Chemical FDA UDI

Category: Ultrasonic dental scaling/debridement system

EndoActivator by Tulsa Dental Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Tulsa Dental Products Llc

Sources (1)

FDA UDI cdb37a2a-fdd4-4412-8b5c-287b913fcdf7 34 fields · synced Jun 8, 2026