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St100

FDA UDI

Class II (US FDA UDI)

by Osada Electric Co., Ltd.

Identity

Trade Name
ST100 FDA UDI
Generic Name
Dental ultrasonic surgical system handpiece tip FDA UDI
Model / Reference
ST100 FDA UDI

Identifiers

Catalog Number
53312 FDA UDI
Primary DI / UDI-DI
04582227425157 FDA UDI
510(k) Number
K844250 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Dental ultrasonic surgical system handpiece tip 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental ultrasonic surgical system handpiece tip

St100 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 handpiece tip.

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 7f4cc288-73b5-4f92-b95c-a4583c292d35 34 fields · synced Jun 8, 2026