Implex Corp.
United StatesFDA applicant, unverified
- Devices
- 65
What Implex Corp. makes
Implex Corp. manufactures orthopedic implants for spinal and joint reconstruction, including trabecular metal acetabular augments, vertebral body replacements (both trabecular metal and Hydrocel variants), and shoulder solutions such as modified glenoid components. Their portfolio also includes patellar replacements, acetabular revision cups (cemented or cementless), tibial components for knee systems, and ceramic femoral heads. Additional products cover tibial spacers and posterior-stabilized knee components.
All listed devices fall under Class II regulatory classification in the U.S. and are authorised via 510(k) clearance through the FDA. The company operates from the United States, with its devices registered under the relevant U.S. regulatory framework.
Catalogue
Search and filter all 65 devicesShowing 1-50 of 65
Frequently asked questions
How many devices does Implex Corp. have in the registry?
The registry currently lists 65 devices for Implex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Implex Corp.'s devices?
Among its 50 most recently registered devices, Implex Corp. has devices listed in FDA 510(k) (50 devices).
What risk classes do Implex Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Implex Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Implex Corp. in the registry?
The most recently registered devices listed for Implex Corp. include THE TRABECULAR METAL TECHNOLOGY ACETABULAR AUGMENT SYSTEM, MODELS 4893-XX-YY (ZIMMER), 02-212-05XX1 ( IMPLEX), TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1, HYDROCEL VERTEBRAL BODY REPLACEMENT, MODEL 06-172-00XX1 and MODIFICATION TO THE TRABECULAR METAL GLENOID - BIGLIANI/FLATOW THE COMPLETE SHOULDER SOLUTION.