Data / Medical devices / India / Raymond Lifestyle Limited
Raymond Lifestyle Limited: FDA-registered device maker in AURANGABAD Maharashtra, India, 1 510(k) clearance
Raymond Lifestyle Limited is registered with the FDA (registration 8044081) in AURANGABAD Maharashtra, India. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 14, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8044081
- FEI number
- 3002818471
- Address
- Plot No. G-35&36 Midc Ind. Area, Waluj, AURANGABAD Maharashtra, India, 431 136
- Owner or operator
- RAYMOND LIFESTYLE LIMITED (10059137)
- Roles
- Manufacturer
- First device listed
- December 4, 2018
- Registered through
- 2026
- Brand names listed
- kamasutra
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 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 |
|---|---|---|---|---|---|---|
| September 14, 1994 | K931077 | LATEX PROPHYLACTIC RUBBER CONTRACEPTIVE | HIS | Substantially Equivalent | J.K. Chemicals, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 14, 1994. 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.