Medical Device Manufacturer · DE , Tuningen, B.W.

Instrumed International, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2004

7

Total

7

Cleared

0

Denied

Instrumed International, Inc. has 7 FDA 510(k) cleared medical devices. Based in Tuningen, B.W., DE.

Historical record: 7 cleared submissions from 2004 to 2010.

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

7 devices

1–7 of 7

INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054

K100518 · DWP Dilator, Vessel, Surgical · Cardiovascular

INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXX

K100517 · HDA Forceps, Obstetrical · Obstetrics & Gynecology

INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL

K092840 · HCZ Forceps, Surgical, Gynecological · Obstetrics & Gynecology

INSTRUMED VASCULAR CLAMPS

K092544 · DXC Clamp, Vascular · Cardiovascular

INSTRUMED RONGEUR

K081651 · HAE Rongeur, Manual · Neurology

INSTRUMED RETRACTORS

K071771 · GZT Retractor, Self-retaining, For Neurosurgery · Neurology

INSTRUMED LAPAROSCOPE AND ACCESSORIES

K040855 · GEI Electrosurgical, Cutting & Coagulation & Accessories · General & Plastic Surgery