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.
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- 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
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Manufacturer | accessdata.fda.gov |
| Condom With Nonoxynol-9 | LTZ | 2 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 19, 2005 | K051273 | DIVAS DUAL PLEASURE MALE LATEX CONDOM | HIS | Substantially Equivalent | Eagle Twe, Inc. | accessdata.fda.gov |
| April 8, 2003 | K022614 | INVIGRA | HIS | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| March 4, 2002 | K020223 | INVIGRA | HIS | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| March 21, 2000 | K000040 | INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED | HIS | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| March 21, 2000 | K000039 | INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED | HIS | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| March 21, 2000 | K000038 | INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED | HIS | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| December 29, 1999 | K993693 | INVIGRA | HIS | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| August 2, 1999 | K992438 | INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT) | LTZ | Substantially Equivalent | Indus Medicare , Ltd. | accessdata.fda.gov |
| June 15, 1999 | K991374 | INVIGRA | HIS | Substantially Equivalent | Indus 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.