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 3 of 4
DeviceModel / ReferenceRegistriesClassStatus
CH17 contra head CH17
FDA UDI
Class IActive
Csr32 CSR32
FDA UDI
Class IActive
St21 ST21
FDA UDI
Class IIActive
SC point 4 SC point 4
FDA UDI
Class IIActive
Sh27 SH27
FDA UDI
Class IActive
Sh31 SH31
FDA UDI
Class IActive
Plugger set#20 Plugger set#20
FDA UDI
Class IIActive
LHP-12 handpiece LHP-12
FDA UDI
Class IActive
St12d ST12D
FDA UDI
Class IIActive
Golz tip set Golz tip set
FDA UDI
Class IIActive
St38-90r ST38-90R
FDA UDI
Class IIActive
File holder cord File holder cord
FDA UDI
UActive
MCC6 motorcord MCC6
FDA UDI
Class IActive
Lip Clip Lip Clip
FDA UDI
UActive
OSADA Enac PL5 OE-PL5
FDA UDI
Class IIUnknown
St12b ST12B
FDA UDI
Class IIActive
Sh42 SH42
FDA UDI
Class IActive
St83s ST83S
FDA UDI
Class IIActive
CSR32 handpiece CSR32
FDA UDI
Class IUnknown
St70 ST70
FDA UDI
Class IIActive
Sh26 SH26
FDA UDI
Class IActive
St35 ST35
FDA UDI
Class IIActive
Wch-1 WCH-1
FDA UDI
Class IActive
Jch-2 JCH-2
FDA UDI
Class IActive
St25b ST25B
FDA UDI
Class IIActive
St25c ST25C
FDA UDI
Class IIActive
Csr20 CSR20
FDA UDI
Class IActive
SC point 1 SC point 1
FDA UDI
Class IIActive
SH26SP w/1 notch SH26SP
FDA UDI
Class IActive
SC point 5 SC point 5
FDA UDI
Class IIActive
CH07 contra head CH07
FDA UDI
Class IActive
CH21B contra head CH21B
FDA UDI
Class IActive
St84 ST84
FDA UDI
Class IIActive
Osada Xl-S30 XL-S30
FDA UDI
Class IActive
ST109C tip ST109C
FDA UDI
Class IIActive
St94 ST94
FDA UDI
Class IIActive
Diamond file L1 Diamond file L1
FDA UDI
Class IIActive
Plugger set#50 Plugger set#50
FDA UDI
Class IIActive
St15 ST15
FDA UDI
Class IIActive
Osada Enac Oe-505 OE-505
FDA UDI
Class IIActive
St22 ST22
FDA UDI
Class IIActive
St17 ST17
FDA UDI
Class IIActive
CH09 contra head CH09
FDA UDI
Class IActive
Smc-2 SMC-2
FDA UDI
Class IActive
SOH oscillating saw HP SOH
FDA UDI
Class IIActive
MCS6 motorcord MCS6
FDA UDI
Class IActive
SH29S/LVS/MCS8 assy. SH29S/LVS/MCS8
FDA UDI
Class IActive
Pi01-R PI01-R
FDA UDI
Class IIActive
St107 ST107
FDA UDI
Class IIActive
CH24B contra head CH24B
FDA UDI
Class IActive

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