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Data / Medical devices / United States / Little Sparrows Technologies Inc

Little Sparrows Technologies Inc: FDA-registered device maker in Woburn, MA, United States, 1 510(k) clearance

Little Sparrows Technologies Inc is registered with the FDA (registration 3013424071) in Woburn, MA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 5, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3013424071
Address
70 Tower Office Park, Woburn, MA, United States, 01801
Owner or operator
Little Sparrows Technologies Inc (10077317)
Roles
Complaint file establishment, Manufacturer, Manufacturer for export, Specification developer
First device listed
August 21, 2020
Registered through
2026
Brand names listed
bili-hut, bili-hut global, bili-hut™ disposable nest liner & mattress (5-Pack), bili-hut™ fully disposable convenience kit (5-Pack), bili-hut™ fully disposable nest & mattress (3-Pack), bili-hut™ fully disposable nest & mattress (5-Pack), bili-hut™ fully disposable nest mattress cover (15-Pack), bili-hut™ nest frame with one disposable nest liner & mattress and more

Devices it lists

DeviceProduct codeClassRoleSource
Protector, Skin PressureFMP1Complaint file establishment, Manufactureraccessdata.fda.gov
Restraint, ProtectiveFMQ1Complaint file establishment, Manufactureraccessdata.fda.gov
Tester, Color VisionHIT1Complaint file establishment, Manufactureraccessdata.fda.gov
Unit, Neonatal PhototherapyLBI2Complaint file establishment, Manufacturer, Manufacturer for export, Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 5, 2019K190899bili-hutLBISubstantially EquivalentLittle Sparrows Technologies, Inc.accessdata.fda.gov

Compare with other makers

Updated September 5, 2019. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.