Lunar Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lunar Corp. - FDA 510(k) Cleared Devices
Recent clearances: PEDIATRIC REFERENCE DATA, LUNAR REPORT GENERATOR II, PRODIGY LATERAL VIEW SOFTWARE
23
Total
23
Cleared
0
Denied
Lunar Corp. has 23 FDA 510(k) cleared radiology devices. Based in Madison, US.
Historical record: 23 cleared submissions from 1995 to 2000.
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 - Lunar Corp.
23 devices
Cleared
Jul 10, 2000
PEDIATRIC REFERENCE DATA
Radiology
25d
Cleared
Jul 06, 2000
LUNAR REPORT GENERATOR II
Radiology
27d
Cleared
Apr 14, 2000
PRODIGY LATERAL VIEW SOFTWARE
Radiology
31d
Cleared
Dec 08, 1998
PRODIGY TOTAL BODY SOFTWARE
Radiology
56d
Cleared
Dec 08, 1998
ORCA-DX BONE DENSITOMETER
Radiology
47d
Cleared
Nov 18, 1998
FRACTURE RISK ASSESSMENT OPTION FOR PIXI BONE DENSITOMETERS
Radiology
62d
Cleared
Nov 18, 1998
FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER
Radiology
62d
Cleared
Nov 18, 1998
FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERS
Radiology
62d
Cleared
Aug 18, 1998
DPX-RX BONE DENSITOMETER
Radiology
50d
Cleared
Feb 13, 1998
EXPERT-XL LATERAL SPINE BMD ACQUISITION AND ANALYSIS SOFTWARE
Radiology
81d
Cleared
Nov 18, 1997
EXPERT-XL ORTHOPEDIC HIP ACQUISITION AND ANALYSIS SOFTWARE
Radiology
134d
Cleared
Oct 03, 1997
EXPERT-XL TOTAL BODY ACQUISITION AND ANALYSIS SOFTWARE
Radiology
277d