Medical Device Manufacturer · US , Glendale , CA

Osteomed Corp. - FDA 510(k) Cleared Devices

27 submissions · 26 cleared · Since 1991
27
Total
26
Cleared
0
Denied

Osteomed Corp. has 26 FDA 510(k) cleared medical devices. Based in Glendale, US.

Historical record: 26 cleared submissions from 1991 to 2015. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Osteomed Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Osteomed Corp.
27 devices
1-12 of 27
Cleared Jul 15, 2015
OsteoMed Cannulated Screw System
K151021 · HWC
Orthopedic · 90d
Cleared Apr 01, 2003
OSTEOMED CRANIAL FLAP FIXATION SYSTEM
K022277 · GXN
Neurology · 260d
Cleared Nov 26, 2002
INTERPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM
K022887 · KWH
Orthopedic · 88d
Cleared Nov 25, 2002
METATARSOPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM
K022886 · KWH
Orthopedic · 87d
Cleared Oct 18, 2002
1.2MM OSTEOMED AUTO-DRIVE SCREW SYSTEM
K023260 · HWC
Orthopedic · 18d
Cleared Aug 14, 2002
INTRAORAL MANDIBULAR DISTRACTION SYSTEM
K013618 · MQN
Dental · 282d
Cleared Aug 08, 2002
OSA RIGID INTERNAL FIXATION SYSTEM
K021618 · JEY
Dental · 84d
Cleared Jan 16, 2002
OSTEOMED BIORESORBABLE FIXATION SYSTEM
K012486 · DZL
Dental · 167d
Cleared Jul 05, 2001
AUTO-DRIVE LAG SCREW SYSTEM
K010964 · HWC
Orthopedic · 97d
Cleared May 30, 2001
2.0/2.4 CANNULATED SCREW SYSTEM
K010783 · HWC
Orthopedic · 76d
Cleared Jun 16, 1999
OSTEOMED INTRAORAL DISTRACTION SYSTEM
K990944 · MQN
Dental · 86d
Cleared Mar 18, 1998
AUTO-DRIVE BONE SCREW
K974785 · HWC
Orthopedic · 86d
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