Silipos, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Silipos, Inc. makes
Silipos, Inc. manufactures sterile and non-sterile gel sheeting products, including tri-block polymer gel sheets and silicone gel sheeting, as well as soft sock compression garments. These items are designed for medical and therapeutic applications, such as wound care and compression therapy.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) pathway. Products are based in the United States and comply with U.S. regulatory requirements for low-risk devices.
Catalogue
Soft Sock Ref K944240
Regimes: 510(k) Registry: 510(k)Sterilized Tri Block Polymer Gel Sheet Ref K955664
Regimes: 510(k) Registry: 510(k)Tri Block Polumer Gel Sheeting Ref K942695
Regimes: 510(k) Registry: 510(k)Silicone Gel Sheeting Ref K932048
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Silipos, Inc. have in the registry?
The registry currently lists 4 devices for Silipos, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Silipos, Inc.'s devices?
Among its 4 most recently registered devices, Silipos, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Silipos, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Silipos, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Silipos, Inc. in the registry?
The most recently registered devices listed for Silipos, Inc. include SOFT SOCK, STERILIZED TRI BLOCK POLYMER GEL SHEET, TRI BLOCK POLUMER GEL SHEETING and SILICONE GEL SHEETING.