Skip to the page

Data / Medical devices / Jordan / Al Huson Packing Company Limited

Al Huson Packing Company Limited: FDA-registered device maker in Irbid, Jordan, 12 510(k) clearances

Al Huson Packing Company Limited is registered with the FDA (registration 3021389492) in Irbid, Jordan. It lists 2 device types. The FDA files 12 510(k) clearances under its listings, the newest dated August 3, 2023. 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
3021389492
Address
Al Shuna Al Shamalyah Wadi Alryan Jordan Gate Way Project, Irbid, Jordan, 28110
Owner or operator
Al Huson Packing Company Limited (10084049)
Roles
Repackager or relabeler
First device listed
January 12, 2022
Registered through
2026
Brand names listed
Interlude and other Private label brands

Devices it lists

DeviceProduct codeClassRoleSource
Tampon, Menstrual, Scented, Scented-DeodorizedHIL2Repackager or relabeleraccessdata.fda.gov
Tampon, Menstrual, UnscentedHEB2Repackager 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
August 3, 2023K230419Sequel Tampon with Plastic ApplicatorHEBSubstantially EquivalentTampro, Inc.accessdata.fda.gov
October 7, 2019K191431Interlude Rolled Tampons in Plastic ApplicatorHEBSubstantially EquivalentAlbaad Femaccessdata.fda.gov
November 2, 2018K181911Interlude 100% Cotton TamponHEBSubstantially EquivalentAlbaad Femaccessdata.fda.gov
June 15, 2018K173225Interlude and private label Unscented 3-piece compact applicator tamponHEBSubstantially EquivalentAlbaad Femaccessdata.fda.gov
September 22, 2014K140077ALBAAD PLASTIC APPLICATOR TAMPONS UNSCENTEDHEBSubstantially EquivalentAlbaad , Ltd.accessdata.fda.gov
May 28, 2009K090071ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONSHEBSubstantially EquivalentRostam , Ltd.accessdata.fda.gov
December 7, 2006K062001ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONSHEBSubstantially EquivalentRostam , Ltd.accessdata.fda.gov
November 23, 2004K042773ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONSHILSubstantially EquivalentRostam , Ltd.accessdata.fda.gov
May 28, 2004K030474PH BUFFERING PLASTIC APPLICATOR TAMPONHEBSubstantially EquivalentRostam , Ltd.accessdata.fda.gov
May 9, 2002K020535INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONSHEBSubstantially EquivalentRostam , Ltd.accessdata.fda.gov
August 3, 2000K001641TAMPONSHEBSubstantially EquivalentRostam , Ltd.accessdata.fda.gov
February 20, 1997K965064ROSTAM APPLICATOR TAMPON/ROSTAM NON APPLICATOR TAMPONHEBSubstantially EquivalentRostam , Ltd.accessdata.fda.gov

Compare with other makers

Updated August 3, 2023. 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.