Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AbbottLabelled 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 13, 2026, FDA's public records list Jomed with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 23, 2003: JOVUS EAGLE EYE F/X 2.9F IVUS CATHETER, MODEL 85900.
| Date | Record | Source |
|---|---|---|
| Jun 23, 2003 | JOVUS EAGLE EYE F/X 2.9F IVUS CATHETER, MODEL 85900K031346 · OBJ | 510(k) clearances |
| May 28, 2003 | IN-VISION IMAGING SYSTEMK031148 · DXK | 510(k) clearances |
| May 14, 2003 | JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS AG145300,141300,142300,132200,14M350,14M345,14M360,143390,141002K031277 · DQX | 510(k) clearances |
| Mar 31, 2003 | JOSTENT SELFX, MODELS 015SX4406; 015SX4408; 015SX4410; 015SX680; 015SX6808; 015SX6810K030053 · FGE | 510(k) clearances |
| Dec 16, 2002 | JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050K022762 · DQX | 510(k) clearances |
| May 17, 2002 | SMARTWIRE/SMARTMAP PRESSURE SYSTEMK021219 · DQX | 510(k) clearances |
| Apr 11, 2002 | MODIFICATION TO FOX PTA CATHETERK020854 · LIT | 510(k) clearances |
| Jun 21, 2001 | FOX PTA CATHETER, 3.0, 4.0, 5.0, 6.0, 7.0, AND 8.0 X 40 MM, MODELS A14003, A14004, A14005, A14006, A14007, A14008K010838 · DQY | 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
