Respire Medical
Respire Medical holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2013, with 5 FDA device recalls on record.
Top product codes for Respire Medical
FDA recalls by Respire Medical
- Z-1947-2018 — Respire Pink Series EF+ Oral Sleep Apnea Device.
- Z-1948-2018 — Respire Pink+ Hard/Soft Oral Sleep Apnea Device
- Z-1950-2018 — Respire Pink H/S Oral Sleep Apnea Device
- Z-1949-2018 — Respire Pink+ Hard Oral Sleep Apnea Device
- Z-1951-2018 — Respire Pink H/S Oral Sleep Apnea Device
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Respire Medical
Data sourced from openFDA. This site is unofficial and independent of the FDA.