Medical Device Manufacturer · US , Mchenry , IL

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

13 submissions · 13 cleared · Since 1984

Recent clearances: PLANMED NUANCE EXCEL, PLANMECA SOVEREIGN

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.

Planmeca USA, Inc. is one of 14548 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

13 devices

1-12 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

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

Filters