Data / Medical devices / United States / Package Solutions, LLC
Package Solutions, LLC: FDA-registered device maker in Pompano Beach, FL, United States, 1 510(k) clearance
Package Solutions, LLC is registered with the FDA (registration 3010142145) in Pompano Beach, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 20, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010142145
- FEI number
- 3006559549
- Address
- 2131 Blount Rd, Pompano Beach, FL, United States, 33069
- Owner or operator
- Package Solutions, LLC (10050462)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- November 19, 2015
- Registered through
- 2026
- Brand names listed
- Adam & Eve Silicone Lube, Adam & Eve Water-Based Forbidden Anal Lube, Adam & Eve Water-Based Lube, Adam & Eve Water-Based Masturbator Lube, Adam & Eve Water-Based Personal Lube, Adam & Eve Water-Based Vibrator Lube, Happy Lube Silicone Personal Lubricant, Happy Lube Water-Based Personal Lubricant and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Manufacturer, 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 20, 2015 | K150153 | Swiss Navy Premium Silicone Lubricant;Swiss Navy Premium Water Based Lubricant;Swiss Navy Premium All Natural Lubricant | NUC | Substantially Equivalent | Package Solutions, LLC | accessdata.fda.gov |
Compare with other makers
Updated October 20, 2015. 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.