Acromed Corp.
United StatesFDA applicant, unverified
- Devices
- 41
What Acromed Corp. makes
Acromed Corp. manufactures spinal fixation and stabilization devices, including anterior cervical stabilization systems, pedicle screws, sublaminar wires, and modular spine connectors like the Isola Tandem Connector and Eye Rod. Their portfolio also includes anterior plate systems, variable screw placement (VSP) spinal fixation components, and multi-segmental anterior spinal fixation devices for surgical use.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Search and filter all 41 devicesFrequently asked questions
How many devices does Acromed Corp. have in the registry?
The registry currently lists 41 devices for Acromed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acromed Corp.'s devices?
Among its 41 most recently registered devices, Acromed Corp. has devices listed in FDA 510(k) (41 devices).
What risk classes do Acromed Corp.'s devices fall under?
Among its 41 most recently registered devices, the classes recorded for Acromed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acromed Corp. in the registry?
The most recently registered devices listed for Acromed Corp. include UNIVERSITY PLATE ANTERIOR SYSTEM, ACROMED DOUBLE SUBLAMINAR WIRE, ISOLA(R) TANDEM CONNECTOR and ACROMED PEDICLE SCREW.