Nice-Pak Products, LLC
Also registered as Nice-Pak Products, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1025121
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pdi Surgical Scrub/Brush T150-70 Ref K833549
Regimes: 510(k) Registry: 510(k)Pdi Surgical Scrub Sponge-Brush-T15070 Ref K810337
Regimes: 510(k) Registry: 510(k)Pdi Prepmaster Wet Pack Patient Prep Kit Ref K840342
Regimes: 510(k) Registry: 510(k)Iso-Care Kit Ref K781539
Regimes: 510(k) Registry: 510(k)Ice-Pak, Pdi Ref K780279
Regimes: 510(k) Registry: 510(k)Pdi Sterile Lubricating Jelly Ref K974768
Regimes: 510(k) Registry: 510(k)Den-Z-Orb Ref K780400
Regimes: 510(k) Registry: 510(k)Pdi Prepmaster Wet Pack Vaginal-X21477 Ref K840343
Regimes: 510(k) Registry: 510(k)Pdi Prepmaster Wet Pack Minor Procedure Ref K840344
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1025121
- Address
- 1 Swan Dr, Smyrna, TN, 37167
Frequently asked questions
How many devices does Nice-Pak Products, LLC have in the registry?
The registry currently lists 9 devices for Nice-Pak Products, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nice-Pak Products, LLC's devices?
Among its 9 most recently registered devices, Nice-Pak Products, LLC has devices listed in FDA 510(k) (9 devices).
What risk classes do Nice-Pak Products, LLC's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Nice-Pak Products, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nice-Pak Products, LLC in the registry?
The most recently registered devices listed for Nice-Pak Products, LLC include PDI SURGICAL SCRUB/BRUSH T150-70, PDI SURGICAL SCRUB SPONGE-BRUSH-T15070, PDI PREPMASTER WET PACK PATIENT PREP KIT and ISO-CARE KIT.