Spiracur, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
What Spiracur, Inc. makes
Spiracur, Inc. manufactures wound care systems and devices designed for closed incision and post-surgical site management, including adhesive-free and secure wound closure solutions.
The company’s portfolio is regulated as Class II medical devices in the US, with products authorised via the FDA’s 510(k) clearance process. These devices are listed under the FDA’s 510(k) registry.
Catalogue
Ci-Snap Wound Care System Ref K111006
Regimes: 510(k) Registry: 510(k)Snap Wound Care System Ref K132080
Regimes: 510(k) Registry: 510(k)SNaP Wound Care System Ref K151710
Regimes: 510(k) Registry: 510(k)Cisnap Closed Incision System Ref K133137
Regimes: 510(k) Registry: 510(k)Snap Wound Care System Ref K113032
Regimes: 510(k) Registry: 510(k)Snap Wound Care System Ref K112341
Regimes: 510(k) Registry: 510(k)Snap (R) Wound Care System Ref K111393
Regimes: 510(k) Registry: 510(k)SNaP Wound Care System Ref K142272
Regimes: 510(k) Registry: 510(k)Snap Wound Care Device Ref DEN080011
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Spiracur, Inc. have in the registry?
The registry currently lists 9 devices for Spiracur, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spiracur, Inc.'s devices?
Among its 9 most recently registered devices, Spiracur, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Spiracur, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Spiracur, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spiracur, Inc. in the registry?
The most recently registered devices listed for Spiracur, Inc. include CI-SNAP WOUND CARE SYSTEM, SNAP WOUND CARE SYSTEM, CISNAP CLOSED INCISION SYSTEM and SNAP (R) WOUND CARE SYSTEM.