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Data / Medical devices / United States / Ids

Ids: FDA-registered device maker in Indianapolis, IN, United States, 1 510(k) clearance

Ids is registered with the FDA (registration 3015146106) in Indianapolis, IN, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 13, 2007. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3015146106
Address
5425 Exploration Drive, Indianapolis, IN, United States, 46241
Owner or operator
IDS (10062213)
Roles
Repackager or relabeler
First device listed
December 3, 2025
Registered through
2026
Brand names listed
Digital Oral Thermometer, Ear Scope / Smart Otoscope, Pulse oximeter

Devices it lists

DeviceProduct codeClassRoleSource
Clinical Electronic ThermometerSDV2Repackager or relabeleraccessdata.fda.gov
OtoscopeERA1Repackager or relabeleraccessdata.fda.gov
OximeterDQA2Repackager or relabeleraccessdata.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
July 13, 2007K063641PC-60, NON-INVASIVEPULSE OXIMETERDQASubstantially EquivalentShenzhen Creative Industry Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated July 13, 2007. 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.