Strukmyer Medical, LLC
United StatesFDA applicant, unverified FDA FEI 3000205837
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Strukmyer Medical, LLC makes
Strukmyer Medical, LLC manufactures sterile water and sterile normal saline (0.9% sodium chloride) solutions in various container sizes, including 100 mL, 250 mL, and 500 mL bottles, as well as 120 mL cups, and also produces the Comatryx OTC device.
The company's devices are classified as Class U and are listed in the FDA 510(k) registry; the manufacturer is based in the United States.
Catalogue
Comatryx OTC Ref K232758
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3000205837
- Address
- 1801 Big Town Blvd Ste 100, MESQUITE, TX, 75149
Frequently asked questions
How many devices does Strukmyer Medical, LLC have in the registry?
The registry currently lists 3 devices for Strukmyer Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Strukmyer Medical, LLC's devices?
Among its 3 most recently registered devices, Strukmyer Medical, LLC has devices listed in FDA 510(k) (3 devices).
What are the newest devices from Strukmyer Medical, LLC in the registry?
The most recently registered devices listed for Strukmyer Medical, LLC include Comatryx OTC, CoMatryx Collagen Wound Dressing 1 gram pouch, CoMatryx Collagen Wound Dressing 1 gram vial, CoMatryx Collagen Wound Dressing 10 gram bottle and USP Sterile Water, 120 mL cup, USP Sterile Normal Saline (0.9% sodium chloride), 120 mL cup, USP Sterile Water, 100 mL, 250 mL and 500 mL bottles, USP Sterile Normal Saline (0.9% sodium chloride), 100 mL, 250 mL and 500 mL bottles.