Pm Devices, Inc.
CanadaFDA applicant, unverified
- Devices
- 4
What Pm Devices, Inc. makes
Pm Devices, Inc. manufactures sterile, single-use protective barrier devices designed for surgical and procedural applications, including the PeriPatch Sheet (various models) and PeriPatch Endo-Sleeve, as well as PeriPatch Sleeve variants (e.g., G35, E35, G45). These products are intended to provide contamination control and patient protection during minimally invasive and open surgical procedures.
The company’s portfolio is classified under FDA Class II medical devices and is listed via 510(k) premarket notifications. The devices are regulated under U.S. jurisdiction and appear in the FDA’s 510(k) database as authorised products.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Peripatch Endo-Sleeve Ref K063556
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pm Devices, Inc. have in the registry?
The registry currently lists 4 devices for Pm Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pm Devices, Inc.'s devices?
Among its 4 most recently registered devices, Pm Devices, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Pm Devices, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Pm Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pm Devices, Inc. in the registry?
The most recently registered devices listed for Pm Devices, Inc. include PERIPATCH SHEET, MODELS 1.5P8, 4P4, 4P6, 6P8, 10P16, 1.5P16, PERIPATCH ENDO-SLEEVE, PERIPATCH SHEET, MODELS 1.5P8, 1.5P16, 4P4, 4P6, 6P8 AND 10P16 and PERIPATCH SLEEVE, MODELS G35, E35, G45, E45, G60, E60, 5C6, 5C8, 5C10.