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.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list AirStrip Technologies with 15 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Dec 9, 2021: AirStrip ONE Web Client with Alarm Communication Management (ACM).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 9, 2021 | AirStrip ONE Web Client with Alarm Communication Management (ACM)K211949 · MSX | 510(k) clearances |
| Sep 11, 2018 | AirStrip RPM InvisionHeart AdapterK182226 · MWI | 510(k) clearances |
| Sep 19, 2016 | AirStrip RPMK160862 · MSX | 510(k) clearances |
| Aug 4, 2016 | AirStrip Sense4Baby Model C Fetal Monitor The Sense4Baby System Model C is indicated for monitoring of maternal and fetal physiologic paClass II · Belt clip may become detached causing electronic components to be exposed. | Device recalls |
| Mar 10, 2015 | Sense4Baby System Model B+ (MSA)K143114 · LQK | 510(k) clearances |
| Feb 14, 2014 | AIRSTRIP REMOTE PATIENT MONITORINGK133450 · MWI | 510(k) clearances |
| Feb 6, 2014 | AIRSTRIP REMOTE PATIENT MONITORINGK133394 · MWI | 510(k) clearances |
| Jul 3, 2013 | AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTERK131786 · MWI | 510(k) clearances |
| Nov 20, 2012 | AIRSTRIP RPM FOR LIFENET CONSULTK121712 · MSX | 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
