Seirin-America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seirin-America, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Seirin-America, Inc. has 4 FDA 510(k) cleared medical devices. Based in Weymouth, US.
Historical record: 4 cleared submissions from 1996 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Seirin-America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seirin-America, Inc.
4 devices
Cleared
Feb 10, 1997
SEIRIN PYONEX ACUPUNCTURE NEEDLES
General Hospital
19d
Cleared
Feb 10, 1997
SEIRIN JR ACUPUNCTURE NEEDLES
General Hospital
18d
Cleared
Oct 16, 1996
SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES
General Hospital
27d
Cleared
Aug 16, 1996
SEIRIN ACUPUNCTURE NEEDLES
General Hospital
29d