Medical Device Manufacturer · US , Mchenry , IL

Planmeca USA, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1984

Total

Cleared

Denied

Planmeca USA, Inc. has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1984 to 2011. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Planmeca USA, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Planmeca USA, Inc.

13 devices

1-13 of 13

PM2002 PROLINE, PM2002 PROLINE EC

PM2002 CC, ARISTOCRAT AND ARISTOCRAT DELUXE

K904947 · BZG

Anesthesiology · 90d

Cleared Jan 30, 1991

PM2002 CC AND PM2002 EC

K904948 · EIA

Dental · 90d

Cleared Nov 26, 1986

DENTAL RADIOGRAPHIC 90, MODEL PM 2002 CC PANORAMIC

K864474 · EHD

Radiology · 13d

Cleared Sep 19, 1984

AUTOMATIC PATIENT CHAIR PM2000 & A

Planmeca USA, Inc. - FDA 510(k) Cleared Devices

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