H.S. Intl. Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
H.S. Intl. Co., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
H.S. Intl. Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Concord, US.
Historical record: 5 cleared submissions from 1989 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by H.S. Intl. Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - H.S. Intl. Co., Inc.
5 devices
Cleared
Feb 27, 1998
FIRE STICK
General & Plastic Surgery
185d
Cleared
Jul 11, 1995
SCISSORS, UNIVERSAL, LAPAROSCOPIC W/MONOPOLAR CAUTERY REUSABLE
General & Plastic Surgery
78d
Cleared
May 19, 1995
CUTTER, VITREOUS ANTERIOR VITRECTOMY PROBE (AVP)
Ophthalmic
81d
Cleared
Feb 03, 1994
DISPOSABLE UNIVERSAL LAPORASCOPIC SCISSORS
General & Plastic Surgery
442d
Cleared
Feb 28, 1989
SHAPIRO CUTTER
Ophthalmic
25d