Medical device makerLabelled 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 Bird Life Design with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 16, 1993: BLD HEATED BREATHING CIRCUIT W/EXHALATION VALVE.
| Dec 16, 1993 | BLD HEATED BREATHING CIRCUIT W/EXHALATION VALVEK931487 · CAI | 510(k) clearances |
| Nov 24, 1993 | BARRIERFLEX-I, AND BARRIERFLES-IIK934189 · CAH | 510(k) clearances |
| Nov 24, 1993 | HME W/O FILTER HYGROFLEX, HYGROFLEX-T, MODIFICATIONK934190 · BYD | 510(k) clearances |
| Oct 19, 1993 | BARRIERFLEX-PF PULMONARY FUNCTION TESTING FILTERK934540 · CAH | 510(k) clearances |
| Oct 15, 1993 | BLD NEONATAL HEATED WIRE BREATHING CIRCUIT- 30 VOLT COMPATIBLEK933641 · CAI | 510(k) clearances |
| Apr 30, 1993 | BLD-18000 SERIES HEATED BREATHING CIRCUITK925543 · CAI | 510(k) clearances |
| Feb 9, 1993 | BABYSET AND PAC (PULMONARY ASSIST CIRCUIT)K930252 · CAI | 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
