Endovations is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endovations - FDA 510(k) Cleared Devices
37
Total
36
Cleared
0
Denied
Endovations has 36 FDA 510(k) cleared gastroenterology & urology devices. Based in Camp Hill, US.
Historical record: 36 cleared submissions from 1986 to 1996.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Endovations
37 devices
Cleared
Feb 08, 1996
ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETER
Gastroenterology & Urology
73d
Cleared
Oct 13, 1994
INJECT-SNARE
Gastroenterology & Urology
164d
Cleared
Feb 28, 1994
ENDOVATIONS(R) .035 PRE-CUT PAPILLATOME
Gastroenterology & Urology
180d
Cleared
Oct 08, 1991
2 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATH
Gastroenterology & Urology
43d
Cleared
Sep 16, 1991
5MM MICROSCISSORS
General & Plastic Surgery
18d
Cleared
Aug 07, 1991
OVAL CUP BIOPSY FORCEP
Gastroenterology & Urology
145d
Cleared
May 31, 1989
ENDO-SPONGE
Gastroenterology & Urology
58d
Cleared
Dec 08, 1988
TRANSENDOSCOPIC ASPIRATION NEEDLE
Gastroenterology & Urology
139d
Cleared
Mar 30, 1988
ENTERON PERCUTAN. ENDOSCOPIC GASTROSTOMY TRAY-PEG
Gastroenterology & Urology
222d
Cleared
Mar 29, 1988
WASHING CATHETER
Gastroenterology & Urology
98d
Cleared
Dec 31, 1987
ENTERON LIVER BIOPSY TRAY
Gastroenterology & Urology
87d
Cleared
Dec 29, 1987
HOLLOW ALLIGATOR GRASPING FORCEP (MODEL 18/12)
Gastroenterology & Urology
89d
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