Manufacturer registered with FDA
New World Imports, Inc.
Nashville, TN, United States. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What New World Imports, Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Over the Counter Denture CleanserEFT · Class 1 | Denture cleansers & adhesives | Maker | Freshmint | 2023 |
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | Freshmint | 1978 |
| Dental FlossJES · Class 1 | Floss & interdental cleaners | Maker | Freshmint | 2022 |
| Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt Denture AdhesiveKOO · Class 1 | Denture cleansers & adhesives | Maker | CareALLFreshmint | 2022 |
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
New World Imports, Inc. 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: Whitehill Oral Technologies, Inc. (1), Procter & Gamble (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 12 Dec 1996 | K963746 | IDS DENTAL FLOSS WITH SODIUM FLUORIDE MICRODENT DENTAL FLOSS WITH SODIUM FLUORIDE AP-24 DENTAL FLOSS WITH SODIUM FLUORID | Whitehill Oral Technologies, Inc. | JES Dental Floss |
| 30 Nov 1994 | K945200 | FIXODENT, FIXODENT FRESH, FASTEETH AND EXTRA HOLD FASTEETH DENTURE ADHESIVCES | Procter & Gamble | KOO Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt Denture Adhesive |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| NEW WORLD IMPORTS, INC.FDA reg. 1044117 | Nashville, TN, United States | Specification developer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 1044117). 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.