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Data / Medical devices / India / Indus Medicare Private Limited

Indus Medicare Private Limited: FDA-registered device maker in Medak District Telangana, India, 9 510(k) clearances

Indus Medicare Private Limited is registered with the FDA (registration 3003759643) in Medak District Telangana, India. It lists 2 device types. The FDA files 9 510(k) clearances under its listings, the newest dated August 19, 2005. 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
3003759643
Address
Ramaipally Village, Medak District Telangana, India, 502 336
Owner or operator
INDUS MEDICARE LIMITED (9036370)
Roles
Manufacturer
First device listed
December 10, 2007
Registered through
2026
Brand names listed
Bare Skin, Black Jack, Desire, Diva's Dual Pleasure, HUSTLER, Hugger, Invigra Super Safe, NOW Carnival and more

Devices it lists

DeviceProduct codeClassRoleSource
CondomHIS2Manufactureraccessdata.fda.gov
Condom With Nonoxynol-9LTZ2Manufactureraccessdata.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 19, 2005K051273DIVAS DUAL PLEASURE MALE LATEX CONDOMHISSubstantially EquivalentEagle Twe, Inc.accessdata.fda.gov
April 8, 2003K022614INVIGRAHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
March 4, 2002K020223INVIGRAHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
March 21, 2000K000040INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVOREDHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
March 21, 2000K000039INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVOREDHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
March 21, 2000K000038INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVOREDHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
December 29, 1999K993693INVIGRAHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
August 2, 1999K992438INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)LTZSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov
June 15, 1999K991374INVIGRAHISSubstantially EquivalentIndus Medicare , Ltd.accessdata.fda.gov

Compare with other makers

Updated August 19, 2005. 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.