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 Johnson & Johnson. FDA records under its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 15, 2026, FDA's public records list Johnson & Johnson Professionals with 206 510(k) clearances. The most recent is a 510(k) clearance dated Apr 7, 2000: SIPHONGUARD CSF CONTROL DEVICE.
| Apr 7, 2000 | SIPHONGUARD CSF CONTROL DEVICEK992173 · JXG | 510(k) clearances |
| Mar 13, 2000 | CODMAN ETHISORB DURA PATCHK991413 · GXQ | 510(k) clearances |
| Jul 9, 1999 | CODMAN MICROSENSOR VENTRICULAR CATHETER KITK991222 · GWM | 510(k) clearances |
| Dec 18, 1998 | SUNDT SLIM-LINE ANEURYSM CLIP APPLIERK982379 · HCI | 510(k) clearances |
| Dec 4, 1998 | G2 TOTAL HIP SYSTEM FEMORAL STEM (11/13 TAPER)K982812 · KWY | 510(k) clearances |
| Nov 6, 1998 | CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESISK983141 · JDB | 510(k) clearances |
| Oct 27, 1998 | SUMMIT ACETABULAR SYSTEMK983014 · LPH | 510(k) clearances |
| Jul 17, 1998 | HAKIM MICRO PROGRAMMABLE VALVE SYSTEMK980778 · JXG | 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
