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., part of Cooper CompaniesLabelled by claude-sonnet-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 15, 2026, FDA's public records list Cabot Medical with 38 510(k) clearances. The most recent is a 510(k) clearance dated Mar 25, 1996: CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT.
| Mar 25, 1996 | CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK960148 · FAD | 510(k) clearances |
| Nov 21, 1995 | CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK946109 · KNS | 510(k) clearances |
| Jul 21, 1995 | CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951972 · FBO | 510(k) clearances |
| Jul 11, 1995 | CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK951714 · GEX | 510(k) clearances |
| Apr 19, 1995 | CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMPK941743 · HIG | 510(k) clearances |
| Mar 15, 1995 | 3000 ELECTRONIC INSUFFLATOR MODIFICATIONK934115 · HIF | 510(k) clearances |
| Jul 27, 1994 | CABOT MEDICAL BIPOLAR CUTTING FORCEPSK932293 · KNS | 510(k) clearances |
| Jun 30, 1994 | THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COVK930954 · HIB | 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
