Ortho Pared Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Ortho Pared Instruments, Inc. makes
Ortho Pared Instruments, Inc. manufactures surgical tools for orthopedic procedures, including meniscus extraction devices, suture passers for tendon and ligament repairs, drill guides for precise bone preparation, and guillotine blades for tissue removal.
The company’s products are regulated under FDA Class I and Class II classifications, with several devices listed via the 510(k) pathway. These instruments are intended for use in orthopedic surgeries and are tracked in the FDA’s 510(k) registry.
Catalogue
Meniscus Extractor Ref K820225
Regimes: 510(k) Registry: 510(k)Universal Suture Passer Ref K812566
Regimes: 510(k) Registry: 510(k)Universall Drill Guide Ref K820226
Regimes: 510(k) Registry: 510(k)Guillotine Blade Ref K831772
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ortho Pared Instruments, Inc. have in the registry?
The registry currently lists 4 devices for Ortho Pared Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ortho Pared Instruments, Inc.'s devices?
Among its 4 most recently registered devices, Ortho Pared Instruments, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Ortho Pared Instruments, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Ortho Pared Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ortho Pared Instruments, Inc. in the registry?
The most recently registered devices listed for Ortho Pared Instruments, Inc. include MENISCUS EXTRACTOR, UNIVERSAL SUTURE PASSER, UNIVERSALL DRILL GUIDE and GUILLOTINE BLADE.