Norland Corp. is one of 20431 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Norland Corp. - FDA 510(k) Cleared Devices
Recent clearances: FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER, FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS, REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER
15
Total
15
Cleared
0
Denied
Norland Corp. has 15 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1979 to 1998.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Norland Corp.
15 devices
Cleared
Jun 12, 1998
FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER
Radiology
137d
Cleared
Jun 12, 1998
FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS
Radiology
119d
Cleared
May 20, 1998
REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER
Radiology
126d
Cleared
Feb 13, 1998
NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS
Radiology
154d
Cleared
Jan 29, 1998
NORLAND MODEL PDEXA BONE DENSITOMETER
Radiology
163d
Cleared
Oct 31, 1997
APOLLO
Radiology
87d
Cleared
Feb 01, 1995
MODEL PDEXA BONE DENSITOMETER
Radiology
649d
Cleared
Sep 23, 1994
FORARM OPT/NORLAND XR SERIES X-RAY BONE DENSITOMET
Radiology
662d
Cleared
Nov 27, 1992
MODEL XCT-900 PQCT X-RAY BONE DENSITOMETER
Radiology
196d
Cleared
Sep 24, 1991
LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET
Radiology
75d
Cleared
Apr 29, 1991
NORLAND XR26 WHOLE BODY OPTION
Radiology
374d
Cleared
Nov 23, 1990
NORLAND XR26 LATERAL SPINE OPTION
Radiology
141d