This page includes the latest FDA filings for American Medical Devices Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
AMERICAN MEDICAL DEVICES, INC. | MOISTAIR FLUID AIR TUBING SET | 1998-02-19 |
AMERICAN MEDICAL DEVICES, INC. | ENDOVIEW SPPHIRE LENS SET | 1997-08-06 |
AMERICAN MEDICAL DEVICES, INC. | ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.) | 1997-06-24 |
AMERICAN MEDICAL DEVICES, INC. | ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.) | 1997-05-20 |
AMERICAN MEDICAL DEVICES, INC. | ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.) | 1997-05-20 |
AMERICAN MEDICAL DEVICES, INC. | ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT | 1997-05-06 |
NCAGE Code | 0KHA5 | AMERICAN MEDICAL DEVICES INC |
NCAGE Code | 1TUQ1 | AMERICAN MEDICAL DEVICES INC |
CAGE Code | 0KHA5 | AMERICAN MEDICAL DEVICES, INC |
CAGE Code | 1TUQ1 | AMERICAN MEDICAL DEVICES, INC. RETINALABS, INC. |