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Data / Medical devices / United States / Natureplex LLC

Natureplex LLC: FDA-registered device maker in Olive Branch, MS, United States, 1 510(k) clearance

Natureplex LLC is registered with the FDA (registration 3003631744) in Olive Branch, MS, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 20, 2018. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003631744
Address
11085 Airport Rd, Olive Branch, MS, United States, 38654
Owner or operator
Natureplex (10095319)
Roles
Manufacturer
First device listed
February 25, 2026
Registered through
2026
Brand names listed
Warm Touch Warming Jelly

Devices it lists

DeviceProduct codeClassRoleSource
Lubricant, PersonalNUC2Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 20, 2018K180828Natureplex Warm Touch Warming JellyNUCSubstantially EquivalentNatureplex, LLCaccessdata.fda.gov

Compare with other makers

Updated December 20, 2018. 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.