Medical Device Manufacturer · US , Washington , DC

Bioscience, Inc. - FDA 510(k) Cleared Devices

4 submissions · 2 cleared · Since 1994
4
Total
2
Cleared
0
Denied

Bioscience, Inc. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1994 to 1996. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Bioscience, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bioscience, Inc.
4 devices
1-4 of 4
Cleared Mar 04, 1996
BIOFIX BIODEGRADABLE MENISCUS ARROW SYSTEM
K955768 · MAI
Orthopedic · 73d
Cleared Jan 31, 1996
BIOFIX BIODEGRADABLE SELF-REINFORCED POLY-L-LACTIDE (SR-PLLA) MINI-TACK
K955003 · MAI
Orthopedic · 91d
Cleared Aug 07, 1995
BIOFIX BIOABSORABABLE SELF-REINFORCED POLY-L-LACTIDE, THREADED FIXATION ROD
K952471 · MAI
Orthopedic · 73d
Cleared Jul 19, 1994
BIOFIX ABSORBABLE SELF-REINFORCED POLY-L-LACTIDE
K925098 · HTY
Orthopedic · 649d
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