Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
690713813

Catalogue (175)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
St72 ST72
FDA UDI
Class IIActive
Diamond file A2 Diamond file A2
FDA UDI
Class IIActive
St106 ST106
FDA UDI
Class IIActive
Y stick Y stick
FDA UDI
UActive
St92 ST92
FDA UDI
Class IIActive
File holder cord File holder cord
FDA UDI
UActive
St100 ST100
FDA UDI
Class IIActive
Osada Endex-Xv OSADA ENDEX-XV
FDA UDI
UActive
Golz tip set Golz tip set
FDA UDI
Class IIActive
L12M micromotor L12M
FDA UDI
Class IActive
Diamond file L2 Diamond file L2
FDA UDI
Class IIActive
Osada Pedo-30w PEDO-30W
FDA UDI
Class IActive
St125 ST125
FDA UDI
Class IIActive
Sm1-03 SM1-03
FDA UDI
Class IActive
AP point 1 AP point 1
FDA UDI
Class IIActive
St07 ST07
FDA UDI
Class IIActive
AP point 2 AP point 2
FDA UDI
Class IIActive
Lhp-12/L12m/Mc12 LHP-12/L12M/MC12
FDA UDI
Class IActive
Jch-1 JCH-1
FDA UDI
Class IActive
St12a ST12A
FDA UDI
Class IIActive
CS132 contra shank CS132
FDA UDI
Class IActive
St16 ST16
FDA UDI
Class IIActive
St91 ST91
FDA UDI
Class IIActive
Osada Enac Oe-F15 OE-F15
FDA UDI
Class IIActive
Osada Xl-S40 XL-S40
FDA UDI
Class IUnknown
CS032 contra shank CS032
FDA UDI
Class IActive
St42b ST42B
FDA UDI
Class IIActive
IM Point IM Point
FDA UDI
Class IIActive
SE-15 handpiece / hose assembly SE-15
FDA UDI
Class IIActive
SH28S/LVS/MCC6 assy. SH28S/LVS/MCC6
FDA UDI
Class IActive
St38-90 ST38-90
FDA UDI
Class IIActive
St08 ST08
FDA UDI
Class IIActive
MCC8 motorcord MCC8
FDA UDI
Class IActive
ST109A tip ST109A
FDA UDI
Class IIActive
CH08 contra head CH08
FDA UDI
Class IActive
Diamond file A3 Diamond file A3
FDA UDI
Class IIActive
St85 ST85
FDA UDI
Class IIActive
St13 ST13
FDA UDI
Class IIActive
LHP-6 handpiece LHP-6
FDA UDI
Class IActive
SE-05 handpiece SE-05
FDA UDI
Class IIActive
Plugger set#15 Plugger set#15
FDA UDI
Class IIActive
Me24 ME24
FDA UDI
Class IActive
SSH saggittal saw HP SSH
FDA UDI
Class IIActive
St75 ST75
FDA UDI
Class IIActive
St73 ST73
FDA UDI
Class IIActive
St82 ST82
FDA UDI
Class IIActive
CSR20L handpiece CSR20L
FDA UDI
Class IUnknown
St23 ST23
FDA UDI
Class IIActive
St12c ST12C
FDA UDI
Class IIActive
St20 ST20
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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