Data / Medical devices / United States / WESTRIDGE LABORATORIES, Inc
WESTRIDGE LABORATORIES, Inc: FDA-registered device maker in Santa Ana, CA, United States, 5 510(k) clearances
WESTRIDGE LABORATORIES, Inc is registered with the FDA (registration 3003169402) in Santa Ana, CA, United States. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated September 27, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003169402
- Address
- 1671 E. Saint Andrew Place, Santa Ana, CA, United States, 92705
- Owner or operator
- Westridge Laboratories, Inc. (10024157)
- Roles
- Contract manufacturer, Manufacturer, Specification developer
- First device listed
- January 8, 2008
- Registered through
- 2026
- Brand names listed
- Adam and Eve Forbidden Anal Lube, Amazon Basics Jelly Water Based Personal Lubricant, Amazon Basics Water Based Personal Lubricant, Analcaine Kick Ass Lube Superior H2O Lubricant, Blissfun Water Based Lubricant, Blowyo Water Based, Body Action Products Ultra Glide water based, Buff Silicone Lubricant and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Specification developer | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Contract manufacturer, 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 27, 2024 | K240745 | ID Free Personal Lubricant | NUC | Substantially Equivalent | Westridge Laboratories, Inc. | accessdata.fda.gov |
| March 9, 2015 | K141767 | ID MILLENNIUM, ID MOMENTS SILICONE | NUC | Substantially Equivalent | Westridge Laboratories, Inc. | accessdata.fda.gov |
| May 1, 2014 | K131866 | SUSTAIN | HIS | Substantially Equivalent | Hollender Sustainable Brands, LLC | accessdata.fda.gov |
| January 14, 2008 | K070511 | RICHTER MALE LATEX CONDOM | HIS | Substantially Equivalent | Richter Rubber Technology Sbn Bhd | accessdata.fda.gov |
| February 15, 2006 | K051295 | I-D GLIDE | NUC | Substantially Equivalent | Westridge Laboratories, Inc. | accessdata.fda.gov |
Compare with other makers
Updated September 27, 2024. 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.