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OSADA ELECTRIC CO., LTD.

US

Last updated May 23, 2026

What OSADA ELECTRIC CO., LTD. makes

OSADA Electric Co., Ltd. manufactures dental and surgical handpieces, including ultrasonic tips for endodontic and periodontal scaling/debridement, remotely-driven dental power tools, and line-powered drilling/sawing systems. Their portfolio also includes endodontic apex locators, diamond files, micromotors, and drive cables for surgical/dental applications. Specific devices range from ultrasonic handpiece attachments like the Golz tip set to corded micromotors such as the L12M and pediatric ultrasonic systems like the OSADA PEDO-30W.

The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with submissions recorded in the FDA’s 510(k) and UDI registries. These products are intended for use in dental and surgical procedures, adhering to regulatory requirements for medical devices in the United States. The manufacturer is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does OSADA Electric Co., Ltd. primarily manufacture?

OSADA Electric Co., Ltd. specializes in dental and surgical handpieces, including ultrasonic tips for endodontic and periodontal procedures like scaling and debridement. Their portfolio also covers remotely-driven dental power tools, line-powered drilling and sawing systems, endodontic apex locators, diamond files, micromotors, and drive cables. These devices are designed for precision applications in dental and surgical settings, such as the OSADA PEDO-30W for pediatric use or the L12M micromotor for controlled drilling.

Where is OSADA Electric Co., Ltd. based, and how does this affect its regulatory compliance?

OSADA Electric Co., Ltd. is based in the United States, which means its devices must comply with FDA regulations. The company’s products are listed in the FDA’s 510(k) and UDI registries, indicating they undergo premarket submissions and unique device identification processes. This ensures traceability and adherence to U.S. medical device standards, though compliance is tied to individual devices, not the company itself.

Which regulatory registries list OSADA Electric Co., Ltd.’s devices, and why?

OSADA Electric Co., Ltd.’s devices appear in the FDA’s 510(k) and UDI registries. The 510(k) pathway is used for devices deemed substantially equivalent to existing approved products, requiring premarket notifications. The UDI system assigns unique identifiers to devices for tracking and regulatory purposes, ensuring transparency in the supply chain and compliance with FDA requirements for medical device traceability.

How are OSADA Electric Co., Ltd.’s devices classified under FDA regulations?

OSADA Electric Co., Ltd.’s devices fall into three FDA classification categories: Class I (generally low-risk, like some handpiece tips), Class II (moderate-risk, such as powered dental tools requiring special controls), and Unclassified (U), which may include experimental or emerging technologies pending final classification. The classification determines the regulatory pathway, with Class II devices often requiring additional validation before market entry.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
690713813

Catalogue (175)

Page 2 of 4
DeviceModel / ReferenceRegistriesClassStatus
St99 ST99
FDA UDI
Class IIActive
Osada Endex Plus EM-S8
FDA UDI
UActive
Diamond file A1 Diamond file A1
FDA UDI
Class IIActive
ST109Btip ST109B
FDA UDI
Class IIActive
Osada Xl-230 XL-230
FDA UDI
Class IActive
Sh42 SH42
FDA UDI
Class IUnknown
Wd-5 WD-5
FDA UDI
Class IActive
L5M micromotor L5M
FDA UDI
Class IActive
St84s ST84S
FDA UDI
Class IIActive
AP set 7 AP set 7
FDA UDI
Class IIActive
Diamond file A set Diamond file A set
FDA UDI
Class IIActive
St108 ST108
FDA UDI
Class IIActive
Surgical tip set (3) Surgical tip set (3)
FDA UDI
Class IIActive
SE-15 handpiece SE-15
FDA UDI
Class IIActive
Osada Exl-M40 EXL-M40
FDA UDI
Class IActive
St70z ST70Z
FDA UDI
Class IIActive
St83 ST83
FDA UDI
Class IIActive
St139 ST139
FDA UDI
Class IIActive
St45 ST45
FDA UDI
Class IIActive
Osada Xl-30w XL-30W
FDA UDI
Class IActive
St97 ST97
FDA UDI
Class IIActive
SRH reciprocating HP SRH
FDA UDI
Class IIActive
MCS8 motorcord MCS8
FDA UDI
Class IActive
SM2L motor SM2L
FDA UDI
Class IActive
St25a ST25A
FDA UDI
Class IIActive
Ach-1 ACH-1
FDA UDI
Class IActive
Sh28s SH28S
FDA UDI
Class IActive
St95 ST95
FDA UDI
Class IIActive
Plugger set#30 Plugger set#30
FDA UDI
Class IIActive
Diamond file S Diamond file S
FDA UDI
Class IIActive
Pi02-R PI02-R
FDA UDI
Class IIActive
Pi02-L PI02-L
FDA UDI
Class IIActive
SC point 4-17 SC point 4-17
FDA UDI
Class IIActive
Sh29s SH29S
FDA UDI
Class IActive
Osada Endex EM-S2
FDA UDI
UActive
CS031 contra shank CS031
FDA UDI
Class IActive
St21b ST21B
FDA UDI
Class IIActive
AP point 3 AP point 3
FDA UDI
Class IIActive
Plugger set#40 Plugger set#40
FDA UDI
Class IIActive
St38-90l ST38-90L
FDA UDI
Class IIActive
OE-11L handpiece OE-11L
FDA UDI
Class IIActive
LVS micromotor LVS
FDA UDI
Class IActive
St93 ST93
FDA UDI
Class IIActive
St87 ST87
FDA UDI
Class IIActive
LHP-6/L5M/MCC6 assy. LHP-6/L5M/MCC6
FDA UDI
Class IActive
St98 ST98
FDA UDI
Class IIActive
St14 ST14
FDA UDI
Class IIActive
Pi01-L PI01-L
FDA UDI
Class IIActive
St09 ST09
FDA UDI
Class IIActive
Osada Enac Oew-10 OEW-10
FDA UDI
Class IIActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Osada Electric Co., Ltd. SHINAGAWA-KU Tokyo · JP FEI 2832