Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Medical Instruments Technology, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 1, 2002: KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHE….
| May 1, 2002 | KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKINK012614 · JOW | 510(k) clearances |
| Feb 28, 2002 | ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDSK012640 · HRX | 510(k) clearances |
| Nov 8, 2001 | REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ARTHROSCOPIC BURSK012624 · HRX | 510(k) clearances |
| Oct 26, 2001 | TOURNIQUET CUFF; PNEUMATIC TOURNIQUETK012632 · KCY | 510(k) clearances |
| Jan 31, 1989 | THE ORTHORANGER II ELECTRONIC GONIOMETERK884611 · KQX | 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
