Medical Device Manufacturer · US , Great Neck , NY

Medical Device Inspection Co., Inc. - FDA 510(k) Cleared Devices

30 submissions · 26 cleared · Since 1990

Recent clearances: J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS, JARIT SURGICAL INSTRUMENTS, THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM

30
Total
26
Cleared
0
Denied

Medical Device Inspection Co., Inc. has 26 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 26 cleared submissions from 1990 to 1995.

Browse the FDA 510(k) cleared devices submitted by Medical Device Inspection Co., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medical Device Inspection Co., Inc.

30 devices
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