Merries International, Inc.
TaiwanFDA applicant, unverified
- Devices
- 2
What Merries International, Inc. makes
Merries International, Inc. manufactures bone graft substitutes, including the MERRIES K-PHATE and the UNI-OSTEO (Model CS30250-CS10102), designed for orthopedic and spinal applications.
These products are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Merries K-Phate Bone Graft Substitute Ref K063157
Regimes: 510(k) Registry: 510(k)Merries Uni-Osteo, Model CS30250-CS10102 Ref K051698
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Merries International, Inc. have in the registry?
The registry currently lists 2 devices for Merries International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Merries International, Inc.'s devices?
Among its 2 most recently registered devices, Merries International, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Merries International, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Merries International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Merries International, Inc. in the registry?
The most recently registered devices listed for Merries International, Inc. include MERRIES K-PHATE BONE GRAFT SUBSTITUTE and MERRIES UNI-OSTEO, MODEL CS30250-CS10102.