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Osada Enac Oe-F15

FDA UDI

Class II (US FDA UDI)

by Osada Electric Co., Ltd.

Identity

Trade Name
OSADA ENAC OE-F15 FDA UDI
Generic Name
Dental ultrasonic surgical system generator FDA UDI
Model / Reference
OE-F15 FDA UDI

Identifiers

Catalog Number
3263 FDA UDI
Primary DI / UDI-DI
04582227426000 FDA UDI
510(k) Number
K844250 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Dental ultrasonic surgical system generator 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Category: Ultrasonic dental scaling/debridement systemDental ultrasonic surgical systemUltrasonic dental scaling/debridement system generatorDental ultrasonic surgical system generator

Osada Enac Oe-F15 by Osada Electric Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental ultrasonic surgical system generator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI be861124-d3fd-445b-8823-df5d162e4081 34 fields · synced Jun 1, 2026