Biosurgical Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Biosurgical Corp. makes
Biosurgical Corp. manufactures medical devices for surgical and procedural applications, including multi-lumen suction syringes for precise fluid management and spray dispersion, as well as fibrin sealant applicators for tissue adhesion. Their products are designed for controlled delivery of sealants and suction during minimally invasive and open surgical procedures.
The company’s portfolio consists of Class II devices, regulated under the FDA’s 510(k) clearance pathway. These products are listed in the FDA’s 510(k) database and are intended for use in the United States.
Catalogue
Multi Lumen Suction Syringe Spray Dispenser Ref K000438
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Biosurgical, Corp. Multi Chamber Suction Syringe Ref K964597
Regimes: 510(k) Registry: 510(k)Sealouette Fibrin Sealant Applicator Ref K992351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biosurgical Corp. have in the registry?
The registry currently lists 4 devices for Biosurgical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biosurgical Corp.'s devices?
Among its 4 most recently registered devices, Biosurgical Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Biosurgical Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Biosurgical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biosurgical Corp. in the registry?
The most recently registered devices listed for Biosurgical Corp. include MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER, SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1, BIOSURGICAL, CORP. MULTI CHAMBER SUCTION SYRINGE and SEALOUETTE FIBRIN SEALANT APPLICATOR.