Peritone Research, Ltd.
Country not established
- Devices
- 2
What Peritone Research, Ltd. makes
Peritone Research, Ltd. makes vaginal chamber devices using Pellethane medical grade 2363 and Monsanto Santoprene materials.
The company's devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Vaginal Chamber Pellethane-Medical Grade 2363 Ref K861858
Regimes: 510(k) Registry: 510(k)Monsanto Santoprene (Peritone Device) Ref K861683
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peritone Research, Ltd. have in the registry?
The registry currently lists 2 devices for Peritone Research, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peritone Research, Ltd.'s devices?
Among its 2 most recently registered devices, Peritone Research, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Peritone Research, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Peritone Research, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peritone Research, Ltd. in the registry?
The most recently registered devices listed for Peritone Research, Ltd. include VAGINAL CHAMBER PELLETHANE-MEDICAL GRADE 2363 and MONSANTO SANTOPRENE (PERITONE DEVICE).