Macropore Biosurgery, Inc.
United StatesFDA applicant, unverified
- Devices
- 17
What Macropore Biosurgery, Inc. makes
Macropore Biosurgery, Inc. manufactures resorbable and non-resorbable surgical barriers, distraction systems, and wound management products. Their portfolio includes bioabsorbable sheets for tissue protection, spinal and orthopedic fixation devices, and systems for lipoplasty and mandibular stabilization. The company also produces cranial fixation devices and hydroabsorbent materials for spinal applications.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Products are primarily intended for surgical use in orthopedics, craniofacial, and soft tissue applications. The company is headquartered in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Macropore Biosurgery, Inc. have in the registry?
The registry currently lists 17 devices for Macropore Biosurgery, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Macropore Biosurgery, Inc.'s devices?
Among its 17 most recently registered devices, Macropore Biosurgery, Inc. has devices listed in FDA 510(k) (17 devices).
What risk classes do Macropore Biosurgery, Inc.'s devices fall under?
Among its 17 most recently registered devices, the classes recorded for Macropore Biosurgery, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Macropore Biosurgery, Inc. in the registry?
The most recently registered devices listed for Macropore Biosurgery, Inc. include MACROPORE FX, PS, NS, LP, MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET, MACROPOREDX DISTRACTOR SYSTEM and MACROPORENS CRANILOC.