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Data / Medical devices / Turkey / Adaptas Pack Ambalaj Sanayi Ve Ticaret Anonim Sirketi

Adaptas Pack Ambalaj Sanayi Ve Ticaret Anonim Sirketi: FDA-registered device maker in Beylikduzu Istanbul, Turkey, 1 510(k) clearance

Adaptas Pack Ambalaj Sanayi Ve Ticaret Anonim Sirketi is registered with the FDA (registration 3045742347) in Beylikduzu Istanbul, Turkey. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 2, 2018. Registered through 2026. FDA data exported November 3, 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
3045742347
Address
Beylikduzu OSB Mermerciler Sanayi Sitesi 5. Cadde No.10, Beylikduzu Istanbul, Turkey, TR-34524
Owner or operator
Adaptas Pack Ambalaj Sanayi ve Ticaret Anonim Sirketi (10095996)
Roles
Exporter to the US
First device listed
June 4, 2026
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Tampon, Menstrual, UnscentedHEB2Exporter to the USaccessdata.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 2, 2018K181911Interlude 100% Cotton TamponHEBSubstantially EquivalentAlbaad Femaccessdata.fda.gov

Compare with other makers

Updated November 2, 2018. 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.