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AirStrip Technologies, Inc.

US

Last updated September 17, 2026

About

AI-powered patient monitoring with near real-time waveforms, alarm management, and predictive analytics. Trusted by 675+ hospitals nationwide.

From the manufacturer's own website. Source

Information

Country
US
Address
2915 W Bitters Rd., SAN ANTONIO, TX, 78248
Website
airstrip.com
Facebook
—
Email
[email protected] (from company website)
Phone
+12108050444 (from company website)
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3006104191
DUNS Number
—

Catalogue (22)

DeviceModel / ReferenceRegistriesClassStatus
AirStrip ONE 2010
FDA UDI
Class IIActive
AirStrip OB Legacy Server 1000
FDA UDI
Class IIActive
AirStrip ONE Web Client 2003
FDA UDI
Class IIActive
AirStrip ONE 2002
FDA UDI
Class IIActive
AirStrip OB Legacy iOS 1001
FDA UDI
Class IIActive
AirStrip ONE 2000
FDA UDI
Class IIActive
AirStrip ONE 2001
FDA UDI
Class IIActive
Airstrip Remote Patient Monitoring K133450
FDA 510(k)
Class IIActive
Airstrip Rpm For Lifenet Consult K121712
FDA 510(k)
Class IIActive
AirStrip ONE Web Client with Alarm Communication Management (ACM) K211949
FDA 510(k)
Class IIActive
AirStrip RPM InvisionHeart Adapter K182226
FDA 510(k)
Class IIActive
Sense4Baby System Model B+ (MSA) K143114
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring (rpm) Remote Data Viewing K122133
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring K133394
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring (rpm) K110503
FDA 510(k)
Class IIActive
Airstrip Ob K090061
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring (rpm) Remote Data Viewing K112235
FDA 510(k)
Class IIActive
Airstrip Ob K090269
FDA 510(k)
Class IIActive
AirStrip RPM K160862
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring (rpm) Remote Data Viewing K121871
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring (rpm) Remote Data Viewing Software, Version 3.1 K100133
FDA 510(k)
Class IIActive
Airstrip Remote Patient Monitoring Philips Adapter K131786
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Aug 4, 2016Z-2829-2016—terminated

Belt clip may become detached causing electronic components to be exposed.