Data / Medical devices / United States / Health Care Products, Inc.
Health Care Products, Inc.: FDA-registered device maker in Coldwater, OH, United States, 3 510(k) clearances
Health Care Products, Inc. is registered with the FDA (registration 3006073016) in Coldwater, OH, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 23, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006073016
- Address
- 410 Nisco ST., Coldwater, OH, United States, 45828
- Owner or operator
- HEALTH CARE PRODUCTS, INC. (9098659)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- March 6, 2007
- Registered through
- 2026
- Brand names listed
- Julie, Krasdale, Market Basket, Parade, Preference, Tampons
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Garment, Protective, For Incontinence | EYQ | 1 | Manufacturer | accessdata.fda.gov |
| Pad, Menstrual, Unscented | HHD | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 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 |
|---|---|---|---|---|---|---|
| April 23, 2014 | K132595 | ONTEX ROLL WADDING PLASTIC APPLICATOR COMPACT SIZE UNSCENTED TAMPONS | HEB | Substantially Equivalent | Ontex Bvba | accessdata.fda.gov |
| August 3, 2000 | K001641 | TAMPONS | HEB | Substantially Equivalent | Rostam , Ltd. | accessdata.fda.gov |
| August 2, 1993 | K920238 | PRIVATE LABELS AND FEMTEX | HEB | Substantially Equivalent | First Quality Hygienic, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Tampon, Menstrual, Unscented
- All makers of Pad, Menstrual, Unscented
- All makers of Garment, Protective, For Incontinence
Updated April 23, 2014. 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.