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Data / Medical devices / United States / Inkwell Global Marketing

Inkwell Global Marketing: FDA-registered device maker in Manalapan, NJ, United States, 1 510(k) clearance

Inkwell Global Marketing is registered with the FDA (registration 3001204077) in Manalapan, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 17, 2017. Registered through 2027. 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
3001204077
Address
600 Madison Avenue, Manalapan, NJ, United States, 07726
Owner or operator
Brandito LLC (10095274)
Roles
Specification developer
First device listed
February 17, 2026
Registered through
2027
Brand names listed
Brandito CPR

Devices it lists

DeviceProduct codeClassRoleSource
Valve, Non-RebreathingCBP2Specification 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
November 17, 2017K171961Compower CPR Mask With Oxygen Port, Compower CPR Mask Without Oxygen Port, Compower Infant CPR Mask, Compower Non-Rebreathing Valve (22mm/15mmOD), Non-Rebreathing Valve (22mm/18.5mm)CBPSubstantially EquivalentXiamen Compower Medical Tech. Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 17, 2017. 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.