Piccguard, LLC
United Statesfrom the FDA registration address FDA FEI 3016472589
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Piccguard, LLC makes
Piccguard, LLC manufactures intravenous catheter injection port guards designed to secure and protect peripheral inserted central catheter (PICC) lines, reducing the risk of accidental dislodgment or contamination during medical procedures.
The company’s products fall under FDA Class II medical devices and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
PiccGuard Ref K191195
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016472589
- DUNS number
- 117382745
- Address
- 529 Ontario Avenue, Sheboygan, WI, 53081
- [email protected]
- Phone
- 918-519-2563
Frequently asked questions
How many devices does Piccguard, LLC have in the registry?
The registry currently lists 4 devices for Piccguard, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Piccguard, LLC's devices?
Among its 4 most recently registered devices, Piccguard, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Piccguard, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Piccguard, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Piccguard, LLC in the registry?
The most recently registered devices listed for Piccguard, LLC include PICC Guard 3, PICC Guard 1, PICC Guard 2 and PiccGuard.