Shinemound Enterprise, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shinemound Enterprise, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Shinemound Enterprise, Inc. has 8 FDA 510(k) cleared medical devices. Based in North Billerica, US.
Historical record: 8 cleared submissions from 1997 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Shinemound Enterprise, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Shinemound Enterprise, Inc.
8 devices
Cleared
Sep 30, 2005
POWDERED LATEX PATIENT EXAMINATION GLOVES
General Hospital
77d
Cleared
Jan 28, 2000
SENSI-PRO, DISPOSABLE PRE-POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES...
General Hospital
43d
Cleared
Jan 20, 2000
SENSI-PRO DISPOSABLE POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES...
General Hospital
34d
Cleared
Oct 27, 1999
SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE...
General Hospital
30d
Cleared
Oct 27, 1999
SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH...
General Hospital
30d
Cleared
Dec 22, 1997
SYNTEX
General Hospital
255d
Cleared
Aug 15, 1997
LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES
General Hospital
72d
Cleared
Mar 27, 1997
POLY-MED
General Hospital
36d