Skip to the page

Data / Medical devices / United States / Tworoger Associates, Ltd.

Tworoger Associates, Ltd.: FDA-registered device maker in New York, NY, United States, 1 510(k) clearance

Tworoger Associates, Ltd. is registered with the FDA (registration 2432426) in New York, NY, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 2000. 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
2432426
Address
594 Broadway, Suite 801, New York, NY, United States, 10012
Owner or operator
Tworoger Associates, LTD. DBA Modo Eyewear (9024852)
Roles
Specification developer
First device listed
January 11, 2023
Registered through
2026
Brand names listed
Modo Eyewear, Readers, Magnifying

Devices it lists

DeviceProduct codeClassRoleSource
Case, Contact LensLRX2Specification developeraccessdata.fda.gov
Spectacle, MagnifyingHOI1Specification 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
June 6, 2000K991206BONASSE CONTACT LENS CASELRXSubstantially EquivalentBonasse Ent. Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 6, 2000. 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.