Search FDA 510(k) Clearance Records

Use this 510(k) search tool to find FDA medical device clearance records by K-number, device name, manufacturer, product code, or regulatory consultant. Explore individual submissions, review timelines, predicate device information, and links to official FDA records. Search the database for free, with no registration required.

176,583 clearances · 1976 to present · Updated monthly from FDA records · Free access · No registration required

42 results for "Medartis AG"

25–42 of 42

Search insights Median review: 90d Cleared: 100% Top manufacturer: Medartis AG Lead specialty: Orthopedic

Cleared Apr 09, 2015

APTUS Foot System

Orthopedic · 206d

Cleared Jun 23, 2014

APTUS ULNA SHORTENING 2.5

Orthopedic · 41d

Cleared Dec 18, 2013

APTUS CANNULATED COMPRESSION SCREWS

Orthopedic · 36d

Cleared Apr 27, 2012

APTUS PROXIMAL HUMERUS SYSTEM

Orthopedic · 105d

Cleared Jan 06, 2012

APTUS WRIST ARTHRODESIS PLATES

Orthopedic · 162d

Cleared Dec 15, 2011

APTUS(R) DISTAL HUMERUS SYSTEM

Orthopedic · 104d

Cleared Jun 28, 2011

APTUS FOOT 3.5 SYSTEM

Orthopedic · 89d

Cleared Jun 02, 2011

APTUS CANNULATED COMPRESSION SCREWS

Orthopedic · 87d

Cleared Jan 24, 2011

APTUS ULNA PLATES

Orthopedic · 73d

Cleared Dec 10, 2010

APTUS 1.5 TRILOCK

Orthopedic · 98d

Cleared Sep 23, 2009

APTUS K-WIRE SYSTEM

Orthopedic · 79d

Cleared Jul 13, 2009

APTUS FOOT SYSTEM

Orthopedic · 55d

Cleared Jul 01, 2009

APTUS 2.0/2.3 FOUR CORNER FUSION PLATE

Orthopedic · 85d

Cleared Apr 23, 2009

APTUS 2.0 RADIAL HEAD SYSTEM

Orthopedic · 105d

Cleared Sep 11, 2007

MODUS TRILOCK 2.0/2.3/2.5

Cleared Nov 24, 1999

MODUS 2.5 MANDIBULAR TRAUMA SET

Cleared Nov 24, 1999

MODUS 2.5 MANDIBULAR RECONSTRUCTION SET

Cleared Sep 17, 1999

MODUS SYSTEM SELF-DRILLING SCREWS

Orthopedic · 87d