Highland / Marietta, Inc. is one of 25868 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Highland / Marietta, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999, ENDOSCOPIC MONOPOLAR FORCEPS-SCISSORS, EMF-2000 TO 2999,ENDOSCOPICS MONOPOLARFOEPS-GRASPERS, EMF-3000 TO 3999, ENDOSCOPO
2
Total
2
Cleared
0
Denied
Highland / Marietta, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mentor, US.
Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Highland / Marietta, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Highland / Marietta, Inc.
2 devices