Data / Medical devices / United States / Lyv Life Inc.
Lyv Life Inc.: FDA-registered device maker in San Francisco, CA, United States, 5 510(k) clearances
Lyv Life Inc. is registered with the FDA (registration 3012097557) in San Francisco, CA, United States. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 7, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012097557
- Address
- 58 West Portal Ave Unit 134, San Francisco, CA, United States, 94127
- Owner or operator
- Lyv Life, Inc. (10050173)
- Roles
- Repackager or relabeler
- First device listed
- November 16, 2020
- Registered through
- 2026
- Brand names listed
- Cora, Cora Bladder Pads, Cora Cup, Cora Disc, Cora Period Pads, Cora Tampons
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tampon, Menstrual, Scented, Scented-Deodorized | HIL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Cup, Menstrual | HHE | 2 | Repackager or relabeler | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Menstrual, Reusable | NUQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Menstrual, Unscented | HHD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| October 7, 2019 | K191431 | Interlude Rolled Tampons in Plastic Applicator | HEB | Substantially Equivalent | Albaad Fem | accessdata.fda.gov |
| March 3, 2017 | K162746 | Ontex and other proprietary names | HEB | Substantially Equivalent | Ontex Bvba | accessdata.fda.gov |
| July 2, 2015 | K151170 | Tosama 100% Organic Cotton Menstrual Tampon | HEB | Substantially Equivalent | Tosama, D.O.O. | accessdata.fda.gov |
| April 23, 2014 | K132595 | ONTEX ROLL WADDING PLASTIC APPLICATOR COMPACT SIZE UNSCENTED TAMPONS | HEB | Substantially Equivalent | Ontex Bvba | accessdata.fda.gov |
| May 28, 2009 | K090071 | ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS | HEB | Substantially Equivalent | Rostam , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Tampon, Menstrual, Unscented
- All makers of Cup, Menstrual
- All makers of Garment, Protective, For Incontinence
- All makers of Pad, Menstrual, Unscented
- All makers of Pad, Menstrual, Reusable
- All makers of Tampon, Menstrual, Scented, Scented-Deodorized
Updated October 7, 2019. 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.