Neimark Labs, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Neimark Labs, Inc. makes
Neimark Labs, Inc. manufactures surgical instruments, including the BenderEv Drill Guide for precise orthopedic drilling and the Carter-Thomason Needle-Point Suture Passer for enhanced tissue handling during surgical procedures.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Benderev Drill Guide Ref K923776
Regimes: 510(k) Registry: 510(k)Carter-Thomason Needle-Point Suture Passer Ref K933536
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neimark Labs, Inc. have in the registry?
The registry currently lists 2 devices for Neimark Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neimark Labs, Inc.'s devices?
Among its 2 most recently registered devices, Neimark Labs, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neimark Labs, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neimark Labs, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neimark Labs, Inc. in the registry?
The most recently registered devices listed for Neimark Labs, Inc. include BENDEREV DRILL GUIDE and CARTER-THOMASON NEEDLE-POINT SUTURE PASSER.