Data / Medical devices / United States / Weiman Products, LLC
Weiman Products, LLC: FDA-registered device maker in Gurnee, IL, United States, 1 510(k) clearance
Weiman Products, LLC is registered with the FDA (registration 1450386) in Gurnee, IL, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 2, 1998. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1450386
- FEI number
- 1416404
- Address
- 755 Tri State Pkwy, Gurnee, IL, United States, 60031
- Owner or operator
- WEIMAN PRODUCTS, LLC (9914067)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 15, 1992
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Detergent | JCB | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Indicator, Physical/Chemical Sterilization Process | JOJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Solvent, Adhesive Tape | KOX | 1 | Manufacturer | accessdata.fda.gov |
| Sterilant, Medical Devices | MED | 2 | Contract manufacturer, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| September 2, 1998 | K974062 | MEDSCI 3% GLUTARALDEHYDE | MED | Substantially Equivalent | Medsci, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Solvent, Adhesive Tape
- All makers of Sterilant, Medical Devices
- All makers of Disinfectant, Medical Devices
- All makers of Indicator, Physical/Chemical Sterilization Process
- All makers of Detergent
Updated September 2, 1998. 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.