Data / Medical devices / Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible / United States
FDA-registered makers of Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible in the United States: 7 establishments
7 establishments in the United States are registered with the FDA to make Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible (product code PEB). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible
- Product code
- PEB
- Country
- United States
Makers of Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| CC Wellness LLC | Valencia, CA, United States | Manufacturer | 3 | February 11, 2022 | 0 | 0 | 0 | api.fda.gov |
| Church & Dwight Co., Inc. | Princeton, NJ, United States | Complaint file establishment, Specification developer | 1 | July 23, 2020 | 0 | 0 | 0 | api.fda.gov |
| Fairhaven Health | Middletown, CT, United States | Complaint file establishment, Specification developer | 1 | April 28, 2017 | 0 | 0 | 0 | api.fda.gov |
| Good Clean Love, Inc. | Eugene, OR, United States | Specification developer | 1 | November 7, 2019 | 0 | 0 | 0 | api.fda.gov |
| Boosted Ecommerce, Inc | Beverly Hills, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONS | Greenville, SC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Swiss-American CDMO,LLC | Carrollton, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.