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 & JohnsonLabelled 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. See the Johnson & Johnson group view.
As of Nov 14, 2026, FDA's public records list Menlo Care with 31 510(k) clearances. The most recent is a 510(k) clearance dated Apr 16, 1997: PICC CATHETER/MIDLINE CATHETER.
| Apr 16, 1997 | PICC CATHETER/MIDLINE CATHETERK964447 · LJS | 510(k) clearances |
| Apr 4, 1996 | MIDMARK MIDLINE CATHETERK951620 · FOZ | 510(k) clearances |
| Apr 6, 1995 | CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAYK945521 · FOZ | 510(k) clearances |
| Mar 29, 1995 | LANDMARK MIDLINE CATHETERK944968 · FOZ | 510(k) clearances |
| Mar 29, 1995 | LANDMARK MIDLINE CATHETERK950737 · FOZ | 510(k) clearances |
| Mar 7, 1995 | PERCUTANEOUS GRAINAGE CATHETERK943893 · LJE | 510(k) clearances |
| Feb 28, 1995 | BILIARY STENTK943143 · FGE | 510(k) clearances |
| May 12, 1994 | SAFE-PICC CATHETERK930048 · FOZ | 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
