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Akita Sumitomo Bakelite Co., Ltd.

JP Last updated 23 Oct 2026

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Devices
0
Registries
FDA
FDA recalls
2

Catalogue0

No devices listed yet from this manufacturer.

FDA recalls2

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2016

    • 9 Sep 2016 Z-0388-2017 Class II Terminated Mislabeled product: Sterilization pouch and carton box labeled as Standard type instead of Jr type-Long
    • 9 Sep 2016 Z-0389-2017 Class II Terminated Mislabeled product: Sterilization pouch and carton labeled as Standard Type instead of Short type

Information

Country
JP
Address
27-4, Aza Nakajimashita, Souzen-machi, Akita
FDA FEI number
3002806337