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 Boston ScientificLabelled 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 15, 2026, FDA's public records list Target Therapeutics with 70 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 1998: DETACHABLE SLICONE BALLOON (DSB).
| Apr 21, 1998 | DETACHABLE SLICONE BALLOON (DSB)K965071 · MZQ | 510(k) clearances |
| Apr 21, 1998 | DETACHABLE SILICONE BALLOON (DSB)K964488 · MZQ | 510(k) clearances |
| Oct 31, 1997 | RETRIEVER IIK964210 · DQO | 510(k) clearances |
| Jul 14, 1997 | GUGLIELMI DETACHABLE COIL (GDC), FIBERED PLATINUM COIL, .035 TYPE, BERENSTEIN LIQUID COIL, FIBERED PLATINUM COILS, ACCEK971395 · DQX | 510(k) clearances |
| Mar 24, 1997 | SPINNAKERK965189 · KRA | 510(k) clearances |
| Feb 26, 1997 | BERENSTEIN COILK964112 · KRD | 510(k) clearances |
| Dec 17, 1996 | GDC PATIENT RETURN ELECTTRODE MODEL 45021K963307 · HCG | 510(k) clearances |
| Sep 20, 1996 | GUGLIELMI DETACHABLE COILK962503 · HCG | 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
