Tyrx Pharma, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Tyrx Pharma, Inc. makes
Tyrx Pharma, Inc. manufactures antimicrobial medical devices, including a coated pacemaker pouch (PIVIT CRM) and antimicrobial surgical mesh (TYRX Surgical Mesh and TYRX Antimicrobial Mesh) designed to reduce infection risk in implanted or surgical applications.
These products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Tyrx Surgical Mesh, Model Smpc-0501 Ref K052864
510(k) 510(k)Tyrx Antimicrobial Mesh Ref K053656
510(k) 510(k)
Frequently asked questions
How many devices does Tyrx Pharma, Inc. have in the registry?
The registry currently lists 3 devices for Tyrx Pharma, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tyrx Pharma, Inc.'s devices?
Among its 3 most recently registered devices, Tyrx Pharma, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Tyrx Pharma, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Tyrx Pharma, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tyrx Pharma, Inc. in the registry?
The most recently registered devices listed for Tyrx Pharma, Inc. include PIVIT CRM (TYRX ANTIMICROBIAL PACEMAKER POUCH), MODEL CMRM-0601, TYRX SURGICAL MESH, MODEL SMPC-0501 and TYRX ANTIMICROBIAL MESH.