Registered with FDA
Quality Packaging Specialists International
Burlington, NJ, United States. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Quality Packaging Specialists International currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Powered ToothbrushJEQ · Class 1 | Toothbrushes | Lister | — | 2016 |
| Anti-Snoring DeviceLRK · Class 2 | Anti-snoring & jaw-repositioning devices | Lister | Pure Sleep (OTC) | 2025 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Quality Packaging Specialists International lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Sleep Science Partners, Inc. (1), Procter & Gamble (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 11 Apr 2019 | K190058 | PureSleep (OTC use) | Sleep Science Partners, Inc. | LRK Anti-Snoring Device |
| 15 Sep 2014 | K141018 | ORAL-B TEST DRIVE POWER BRUSH TRIAL PROGRAM KIT, ORAL-B TEST DRIVE POWER TOOTHBRUSH KIT, ORAL-B TEST DRIVE REFILL KIT | Procter & Gamble | JEQ Powered Toothbrush |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| Quality Packaging Specialists International, LLCFDA reg. 3013445151 | Burlington, NJ, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9067895). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.