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 PhilipsLabelled 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 Avent America, Inc. with 4 510(k) clearances. The most recent is a 510(k) clearance dated Sep 22, 2005: ISIS IQ UNO HANDHELD ELECTRONIC BREAST PUMP, MODEL 101.
| Sep 22, 2005 | ISIS IQ UNO HANDHELD ELECTRONIC BREAST PUMP, MODEL 101K052047 · HGX | 510(k) clearances |
| Aug 29, 2005 | ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100K051413 · HGX | 510(k) clearances |
| Jul 28, 1995 | NIPLETTEK952035 · HGY | 510(k) clearances |
| Oct 5, 1994 | AVENT NIPPLE SHIELDK944117 · HFS | 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
