Medical Device Manufacturer · US , Mchenry , IL

Norland Corp. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1979

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

View 15 510(k) Devices ↓

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Norland Corp. Radiology ✕

15 devices

1-12 of 15

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

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