Data / Medical devices / United States / The Honey Pot Company LLC
The Honey Pot Company LLC: FDA-registered device maker in Atlanta, GA, United States, 4 510(k) clearances
The Honey Pot Company LLC is registered with the FDA (registration 3014829931) in Atlanta, GA, United States. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated October 7, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014829931
- Address
- 1115 Howell Mill Rd NW Suite 750, Atlanta, GA, United States, 30318
- Owner or operator
- The Honey Pot Company LLC (10058497)
- Roles
- Complaint file establishment
- First device listed
- September 7, 2023
- Registered through
- 2026
- Brand names listed
- Calming Long Liner 30 CT, Calming Overnight Pad 12 CT, Calming Regular Pad 20 CT, Calming Super Pad 16 CT, Cooling Heavy Flow Daytime Pads 14 CT, Cooling Heavy Flow Overnight Pad 11 CT, Cooling Incontinence Daytime 16 CT, Cooling Incontinence Liner 20 CT and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tampon, Menstrual, Scented, Scented-Deodorized | HIL | 2 | Complaint file establishment | accessdata.fda.gov |
| Cup, Menstrual | HHE | 2 | Complaint file establishment | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Complaint file establishment | accessdata.fda.gov |
| Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile | NRC | 1 | Complaint file establishment | accessdata.fda.gov |
| Pad, Menstrual, Unscented | HHD | 1 | Complaint file establishment | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Complaint file establishment | 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 7, 2019 | K191431 | Interlude Rolled Tampons in Plastic Applicator | HEB | Substantially Equivalent | Albaad Fem | accessdata.fda.gov |
| November 14, 2018 | K182105 | JO Naturalove Personal Lubricant, JO Naturalove Strawberry Fields Flavored Personal Lubricant | NUC | Substantially Equivalent | United Consortium | accessdata.fda.gov |
| August 27, 2018 | K181408 | JO Classic Hybrid Personal Lubricant | NUC | Substantially Equivalent | United Consortium | accessdata.fda.gov |
| November 23, 2004 | K042773 | ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS | HIL | Substantially Equivalent | Rostam , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Cup, Menstrual
- All makers of Pad, Menstrual, Unscented
- All makers of Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile
- All makers of Tampon, Menstrual, Unscented
- All makers of Tampon, Menstrual, Scented, Scented-Deodorized
- All makers of Lubricant, Personal
Updated October 7, 2019. 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.