YDM CORPORATION

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
80439923003928976YDM CORPORATION1N2026-01-0128 IMAIZUMI, HIGASHIMATSUYAMA-SHI Saitama JP 355-0042

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
04963931271214NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271221NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271238NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271245NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271252NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271269NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271276NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp
04963931271283NA - The device is an instrument used when treating patients with reinfected root canal to remove gutta percha, etc. attached to the root canal walls.+819019940653jumpei@ydm.co.jp

Registered Device Listings#

GUDID#

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