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Data / Medical devices / United States / Barbaras Development, Inc.

Barbaras Development, Inc.: FDA-registered device maker in Thousand Oaks, CA, United States, 1 510(k) clearance

Barbaras Development, Inc. is registered with the FDA (registration 3007207474) in Thousand Oaks, CA, United States. It lists 22 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 4, 2025. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3007207474
Address
2545 W Hillcrest Dr Ste 215, Thousand Oaks, CA, United States, 91320
Owner or operator
Barbaras Development, Inc. (10026520)
Roles
Contract manufacturer, Manufacturer for export, Specification developer
First device listed
August 15, 2014
Registered through
2026
Brand names listed
0184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling line, CO2 Sampling Line for Non Breaking Oxygen, Cuffs, DJO, DONJOY, Donjoy, Donjoy, ISOFORM, ECONO BREG/OPTIFLEX and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, TractionILZ1Contract manufactureraccessdata.fda.gov
Accessory, Surgical ApparelLYU1Contract manufactureraccessdata.fda.gov
Airway, NasopharyngealBTQ1Contract manufactureraccessdata.fda.gov
Airway, Oropharyngeal, AnesthesiologyCAE1Contract manufactureraccessdata.fda.gov
Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK2Manufacturer for export, Specification developeraccessdata.fda.gov
Cannula, Nasal, OxygenCAT1Contract manufactureraccessdata.fda.gov
Components, ExerciseIOD1Contract manufactureraccessdata.fda.gov
Device, Intravascular Catheter SecurementKMK1Contract manufactureraccessdata.fda.gov
Insoles, MedicalKYS1Contract manufacturer, Manufacturer for exportaccessdata.fda.gov
Joint, Ankle, External BraceITW1Contract manufactureraccessdata.fda.gov
Joint, Knee, External BraceITQ1Contract manufactureraccessdata.fda.gov
Mask, OxygenBYG1Contract manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Contract manufactureraccessdata.fda.gov
Orthosis, CervicalIQK1Contract manufactureraccessdata.fda.gov
Orthosis, Limb BraceIQI1Contract manufactureraccessdata.fda.gov
Orthosis, LumbarIQE1Manufacturer for exportaccessdata.fda.gov
Pack, Heat, MoistIMA1Contract manufactureraccessdata.fda.gov
Protector, Skin PressureFMP1Contract manufactureraccessdata.fda.gov
Shoe, CastIPG1Contract manufactureraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Contract manufactureraccessdata.fda.gov
Support, ArmIOY1Contract manufactureraccessdata.fda.gov
System, Urine Drainage, Closed, For Non-Indwelling Catheter, Non-SterileNNZ1Contract manufactureraccessdata.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
June 4, 2025K2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineCCKSubstantially EquivalentBarbaras Development, Inc.accessdata.fda.gov

Compare with other makers

Updated June 4, 2025. 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.