R.K. Manufacturing
Also registered as Rk Manufacturing Corporation
Country not established FDA establishment FEI 3002680121
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Rondek PGA Suture (Beige or Violet) Ref K180625
510(k) 510(k)
Company details
- FDA FEI number
- 3002680121
- Address
- 34 Executive Drive, Danbury, CT, 06810
Frequently asked questions
How many devices does R.K. Manufacturing have in the registry?
The registry currently lists 1 device for R.K. Manufacturing. Devices recorded under merged duplicate company entries are counted once.
Which registries list R.K. Manufacturing's devices?
Among its 1 most recently registered device, R.K. Manufacturing has devices listed in FDA 510(k) (1 device).
What risk classes do R.K. Manufacturing's devices fall under?
Among its 1 most recently registered device, the classes recorded for R.K. Manufacturing's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from R.K. Manufacturing in the registry?
The most recently registered devices listed for R.K. Manufacturing include Rondek PGA Suture (Beige or Violet).