Medical Device Manufacturer · US , Mchenry , IL

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

59 submissions · 57 cleared · Since 1977

Recent clearances: PHOTAC-FIL APLICAP, SONO(R) -CEM, PHOTAC-BOND APLICAP, MODIFICATION

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.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

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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