Medical Device Manufacturer · US , Mchenry , IL

Espe GmbH (Us) - FDA 510(k) Cleared Devices

59 submissions · 57 cleared · Since 1977

Total

Cleared

Denied

Espe GmbH (Us) has 57 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 57 cleared submissions from 1977 to 1993.

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Espe GmbH (Us) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Espe GmbH (Us)

59 devices

1-12 of 59

PHOTAC-BOND APLICAP, MODIFICATION

PERTAC UNIVERSAL BOND

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Espe GmbH (Us) - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Espe GmbH (Us)

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