Poly-Medics, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Poly-Medics, Inc. makes
Poly-Medics, Inc. manufactures resorbable orthopedic fixation devices, including granular hard tissue replacement materials and suture anchors for surgical applications. Their portfolio includes trauma plating systems and pop rivets designed for internal fixation, as well as lactose-based anchors for tendon or ligament reattachment.
The company’s devices are classified as Class II under FDA regulations and are recorded in the 510(k) clearance database. Poly-Medics, Inc. is headquartered in the United States.
Catalogue
Hard Tissue Replacement (Htr) Granular Ref K934861
Regimes: 510(k) Registry: 510(k)Lactosorb Suture Anchor Ref K954443
Regimes: 510(k) Registry: 510(k)Lactosorb Trauma Plating System Ref K960988
Regimes: 510(k) Registry: 510(k)Lactosorb Trauma Plating System Ref K955729
Regimes: 510(k) Registry: 510(k)Lactosorb Pop Rivet Ref K951658
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Poly-Medics, Inc. have in the registry?
The registry currently lists 5 devices for Poly-Medics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Poly-Medics, Inc.'s devices?
Among its 5 most recently registered devices, Poly-Medics, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Poly-Medics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Poly-Medics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Poly-Medics, Inc. in the registry?
The most recently registered devices listed for Poly-Medics, Inc. include HARD TISSUE REPLACEMENT (HTR) GRANULAR, LACTOSORB SUTURE ANCHOR, LACTOSORB TRAUMA PLATING SYSTEM and LACTOSORB POP RIVET.