Barnhardt Mfg. Co.
Country not established FDA establishment FEI 1010842
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Barnhardt Mfg. Co. makes
Barnhardt Mfg. Co. manufactures a radiopaque surgical sponge gauze designed for use in operative settings.
The product is classified as a Class U device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Sponge Surgical Guaze Radiopaque Ref K802504
510(k) 510(k)
Company details
- FDA FEI number
- 1010842
- Address
- 1100 Hawthorne Ln, CHARLOTTE, NC, 28205
Frequently asked questions
How many devices does BARNHARDT MFG. CO. have in the registry?
The registry currently lists 1 device for BARNHARDT MFG. CO.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BARNHARDT MFG. CO.'s devices?
Among its 1 most recently registered device, BARNHARDT MFG. CO. has devices listed in FDA 510(k) (1 device).
What are the newest devices from BARNHARDT MFG. CO. in the registry?
The most recently registered devices listed for BARNHARDT MFG. CO. include SPONGE SURGICAL GUAZE RADIOPAQUE.