Holco Instrument Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Holco Instrument Corp. makes
Holco Instrument Corp. manufactures resurface prostheses specifically designed for hip joint replacements, along with a range of surgical and diagnostic instruments for medical procedures.
Their portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) clearance pathway. The company is based in the United States.
Catalogue
Resurface Prostheses For Hip Joint Ref K761324
Regimes: 510(k) Registry: 510(k)Various Surg. & Diagnostic Instru. Etc. Ref K770428
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Holco Instrument Corp. have in the registry?
The registry currently lists 2 devices for Holco Instrument Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Holco Instrument Corp.'s devices?
Among its 2 most recently registered devices, Holco Instrument Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Holco Instrument Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Holco Instrument Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Holco Instrument Corp. in the registry?
The most recently registered devices listed for Holco Instrument Corp. include RESURFACE PROSTHESES FOR HIP JOINT and VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC..