Anspach Mfg., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Anspach Mfg., Inc. makes
Anspach Mfg., Inc. manufactures orthopedic fixation devices, including bone rivets and suture anchors, as well as surgical tools like diffuser filters and cup outs designed for orthopedic procedures.
The company’s products are regulated under FDA Class I and Class II classifications, with some devices requiring 510(k) clearance. These items are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Filter, Diffuser Ref K940276
Regimes: 510(k) Registry: 510(k)Cup Out Ref K905027
Regimes: 510(k) Registry: 510(k)Anspach Bone Rivet, Anspach Suture Anchor Ref K925328
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anspach Mfg., Inc. have in the registry?
The registry currently lists 3 devices for Anspach Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anspach Mfg., Inc.'s devices?
Among its 3 most recently registered devices, Anspach Mfg., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Anspach Mfg., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Anspach Mfg., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anspach Mfg., Inc. in the registry?
The most recently registered devices listed for Anspach Mfg., Inc. include FILTER, DIFFUSER, CUP OUT and ANSPACH BONE RIVET, ANSPACH SUTURE ANCHOR.