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Osada Pedo-30W

by Osada Electric Co., Ltd.

Osada Pedo-30W (3121) is a Class I device made by Osada Electric Co., Ltd., listed in FDA GUDID since 29 Sep 2016 (UDI-DI 04580406860485), registry data as of 1 Jun 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 1 Jun 2026.

Regulatory status

as of registry sync 1 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04580406860485 UDI-DI Date29 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Dental power tool system, line-powered
Model / Ref / Catalog
PEDO-30W, 3121
Primary DI / UDI-DI
04580406860485
FDA product code
EKX
GMDN term
Dental power tool system, line-powered
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EKX (HANDPIECE, DIRECT DRIVE, AC-POWERED).

Other devices from Osada Electric Co., Ltd.

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  • ST106

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See all devices from Osada Electric Co., Ltd. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)