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Data / Medical devices / United States / WTFN Inc. Dba Classic Erotica

WTFN Inc. Dba Classic Erotica: FDA-registered device maker in Chatsworth, CA, United States, 1 510(k) clearance

WTFN Inc. Dba Classic Erotica is registered with the FDA (registration 3009599096) in Chatsworth, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 17, 2016. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3009599096
Address
20950 Lassen St, Chatsworth, CA, United States, 91311
Owner or operator
WTFN INC. DBA CLASSIC BRANDS (10040725)
Roles
Specification developer
First device listed
March 23, 2020
Registered through
2026
Brand names listed
Intimd Crazy Girl Oral Gel, Intimd TASTY Strawberry Oral Gel, Intimd TASTY Watermelon Oral Gel

Devices it lists

DeviceProduct codeClassRoleSource
Lubricant, PersonalNUC2Specification developeraccessdata.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
August 17, 2016K161385Just Like Me Personal LubricantNUCSubstantially EquivalentWtfn-Dba Classic Erotica/Holiday Productsaccessdata.fda.gov

Compare with other makers

Updated August 17, 2016. 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.