Manufacturer registered with FDA
Allied Hill Enterprises, Ltd.
KOWLOON, Hong Kong SAR China. Lists 7 dental device types with FDA across 2 registered establishments, and holds 1 510(k) clearance as applicant.
- Device types listed
- 7
- Brands and models
- 10
- 510(k) clearances
- 12009–2009
- Markets registered in
- 1United States
- Establishments
- 2China, Hong Kong SAR China
510(k) clearances per year, 2000–2026
Devices listed with FDA
What Allied Hill Enterprises, Ltd. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Oral Hygiene Rubber TipJEW · Class 1 | Floss & interdental cleaners | Maker | Oral Care Kits | 2013 |
| Fluid-Filled Teething RingKKO · Class 2 | — | Maker | Handi-craft waterfill teetherSassy Waterfill teethers | 2020 |
| Teething Ring Non-Fluid FilledMEF · Class 1 | — | Maker | Doctor Brown Teether (normal)SASSY BABY, INC | 2008 |
| Mouth MirrorEAX · Class 1 | Dental hand instruments | Maker | baby mouth mirrorDENTAL MIRROR | 2007 |
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | Toothbrush | 2007 |
| Powered ToothbrushJEQ · Class 1 | Toothbrushes | Maker | GENTLE VIBRATIONS TOOTHBRUSH | 2007 |
| Massaging PickJET · Class 1 | Floss & interdental cleaners | Maker | GUM STIMULATOR | 2007 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names Allied Hill Enterprises, Ltd. as the applicant, including filings under its other names.
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| Allied Hill Enterprises, Ltd.FDA reg. 3010337881 | Hong Kong, Hong Kong SAR China | Foreign exporter |
| Essentia Industries Ltd.FDA reg. 3009124884 | Dong Guan Guangdong, China | Contract manufacturer, Foreign exporter, Manufacturer, Repacker / relabeler |
Other names on FDA records
Essentia Industries Ltd.
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9101920). 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.