Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Instrumed International with 38 device recalls and 7 510(k) clearances. The most recent is a device recall dated Sep 8, 2014: D'errico perforator drills are bone cutting and drilling instruments that are used witho….
| Sep 8, 2014 | D'errico perforator drills are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold undeClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | A zipser clamp is an instrument used to compress reduce blood flow to the penis and reduce pain and is sold under the Medline Industries, BoClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | McKenzie enlarging burrs are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under Class II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | Gardner-Wells traction tongs are skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g., fracture or disloClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | Hudson cranial drill sets (w/ brace and 5 attachments) are bone cutting and drilling instruments that are used without a power source on a pClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | A uterine tenaculum is a hook-like instrument used to seize and hold the cervix or fundus sold under the CareFusion, Teleflex Medical, SymmeClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | Schoitz weights are manual devices used with Schoitz tonometers and are intended to measure intraocular pressure by applying a known force oClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Sep 8, 2014 | A circumcision clamp is an instrument used to compress the foreskin of the penis during circumcision of a male infant sold under the MedlineClass II · The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices | Device recalls |
| Aug 31, 2010 | INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054K100518 · DWP | 510(k) clearances |
| Apr 29, 2010 | INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXXK100517 · HDA | 510(k) clearances |
| Dec 3, 2009 | INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICALK092840 · HCZ | 510(k) clearances |
| Oct 26, 2009 | INSTRUMED VASCULAR CLAMPSK092544 · DXC | 510(k) clearances |
| Aug 8, 2008 | INSTRUMED RONGEURK081651 · HAE | 510(k) clearances |
| Aug 2, 2007 | INSTRUMED RETRACTORSK071771 · GZT | 510(k) clearances |
| Apr 16, 2004 | INSTRUMED LAPAROSCOPE AND ACCESSORIESK040855 · GEI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
