Data / Medical devices / United States / Lil Drug Store Products, Inc.
Lil Drug Store Products, Inc.: FDA-registered device maker in Cedar Rapids, IA, United States, 4 510(k) clearances
Lil Drug Store Products, Inc. is registered with the FDA (registration 3003491851) in Cedar Rapids, IA, United States. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 9, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3003491851
- Address
- 9300 Earhart Lane SW, Cedar Rapids, IA, United States, 52404
- Owner or operator
- LIL DRUG STORE PRODUCTS, INC. (9054632)
- Roles
- Repackager or relabeler
- First device listed
- August 30, 2022
- Registered through
- 2026
- Brand names listed
- Eroxon Erectile Dysfunction Gel, Lifestyles Large Latex Condom, 3ct, Lifestyles Ultra-Ribbed Latex Condom, 3ct, Lifestyles Ultra-Sensitive Latex Condom, 3ct, SKYN Elite Large Non-Latex Condom, 3ct, SKYN Elite Non-Latex Condom, 3ct, SKYN Original Non-Latex Condom,3ct
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Repackager or relabeler | accessdata.fda.gov |
| Condom With Nonoxynol-9 | LTZ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Condom, Synthetic | MOL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Non-Medicated Topical Formulation For Treatment Of Erectile Dysfunction. | QWW | 2 | 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 |
|---|---|---|---|---|---|---|
| June 9, 2023 | DEN220078 | Eroxon | QWW | Unknown | Futura Medical Developments Limited | accessdata.fda.gov |
| August 2, 2017 | K171172 | Skyn Original Polyisoprene Lubricated Male Condom - Flavored | MOL | Substantially Equivalent | Ansell Healthcare Products, LLC | accessdata.fda.gov |
| July 31, 2000 | K001883 | LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM | HIS | Substantially Equivalent | Ansell Healthcare, Inc. | accessdata.fda.gov |
| December 6, 1995 | K941258 | LATEX CONDOM | HIS | Substantially Equivalent | Suretex, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 9, 2023. 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.