Lunar Corp.
Madison, WI, US
Lunar Corp. appears in FDA device records in Madison, WI. FDA records list 29 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 29
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 29 510(k) clearances for Lunar Corp. between 1989 and 2000. The busiest year on record is 1998, with 7. The most recent is 2000, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 1 |
| 1990 | 2 |
| 1991 | 1 |
| 1992 | 2 |
| 1995 | 4 |
| 1996 | 4 |
| 1997 | 5 |
| 1998 | 7 |
| 2000 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K001812 | PEDIATRIC REFERENCE DATA | KGI | Substantially Equivalent | |
| K001756 | LUNAR REPORT GENERATOR II | KGI | Substantially Equivalent | |
| K000826 | PRODIGY LATERAL VIEW SOFTWARE | KGI | Substantially Equivalent | |
| K983724 | ORCA-DX BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K983564 | PRODIGY TOTAL BODY SOFTWARE | KGI | Substantially Equivalent | |
| K983271 | FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERS | KGI | Substantially Equivalent | |
| K983269 | FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K983262 | FRACTURE RISK ASSESSMENT OPTION FOR PIXI BONE DENSITOMETERS | KGI | Substantially Equivalent | |
| K982267 | DPX-RX BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K974437 | EXPERT-XL LATERAL SPINE BMD ACQUISITION AND ANALYSIS SOFTWARE | KGI | Substantially Equivalent | |
| K972517 | EXPERT-XL ORTHOPEDIC HIP ACQUISITION AND ANALYSIS SOFTWARE | KGI | Substantially Equivalent | |
| K965226 | EXPERT-XL TOTAL BODY ACQUISITION AND ANALYSIS SOFTWARE | KPS | Substantially Equivalent | |
| K972053 | PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM | KGI | Substantially Equivalent | |
| K970224 | PIXI BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K964307 | EXPANDED REFERENCE VALUES FOR DPX BON DENSITOMETERS | KGI | Substantially Equivalent | |
| K964263 | EXPERT-KL AND HAND ACQUISITION AND ANALYSIS SOFTWARE | KGI | Substantially Equivalent | |
| K961007 | EXPERT SPINE MORPHOTIETRY REFERENCE | KGI | Substantially Equivalent | |
| K961944 | LUNAR REPORT GENERATOR | KGI | Substantially Equivalent | |
| K960907 | ORCA | OXO | Substantially Equivalent | |
| K953032 | LUNAR DPX DENSITOMETER | KGI | Substantially Equivalent | |
| K935454 | DPX TISSUE QUANTIFICATION OUTPUT | JAK | Substantially Equivalent | |
| K950611 | EXPERT MORPHOMERTY SOFTWARD | KGI | Substantially Equivalent | |
| K945526 | LUNAR EXPERT | KGI | Substantially Equivalent | |
| K915535 | FOREARM SOFTWARE FOR LUNAR DPX SERIES BONE DESITOM | KGI | Substantially Equivalent | |
| K914404 | ORTHO SOFTWARE USED W/LUNAR DPX/DPX-L/DPS-@ DESIT | KGI | Substantially Equivalent | |
| K905291 | LATERAL SPINE DETERMAINATIONS DPX/DPX-L/DPX-ALPHA | KGI | Substantially Equivalent | |
| K904980 | DPX-L AND DPX-ALPHA, MODIFICATION | KGI | Substantially Equivalent | |
| K890121 | MODIFIED DPX BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K884625 | DPX BONE DENSITOMETER FOR TOTAL BODY BONE DENSITY | KGI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Claiming lets Lunar Corp. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
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Data as of , FDA export datePage updated Source: openFDA, public domain
