Manufacturer registered with FDA
Shenzhen LYA Silicone Rubber Products Co.,Ltd
Shenzhen, China. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 15
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1China
Devices listed with FDA
What Shenzhen LYA Silicone Rubber Products Co.,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 |
|---|---|---|---|---|
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | First Toothbrush, 309301-920-33Learning Toothbrush , 305300-200-34, 305300-602-34, 305300-500-34, 305300-920-34, 305300-531-34Silicone Toothbrush, 309300-920-33Teether Toothbrush, 305303-000-33 | 2019 |
| Teething Ring Non-Fluid FilledMEF · Class 1 | — | Maker | Cleaning Teether, 385301-400-33, 385301-2010-33Everyday Teether, 222391-905-33, 222391-906-33, 222391-907-33, 222391-904-33,First Teether, 385372-200-33, 385372-600-33, 385372-920-33, 385372-883-33, 385364-819-33,Front & Side Teether, 385302-500-34, 385302-5005-34Molar Teether, 385300-602-36, 385300-6046-36Ring Teether, 385632-001-33Silicone Fruit Teether, 385362-116-33, 385362-287-33, 385362-410-33, 385362-590-33,222391-531-33, 222391-883-33, 221040-575-34, 221040-676-34, 221040-274-34, 221040-920-34222903-000-26, 222903-684-26, 222903-616-26, 222903-242-26, 222901-920-26385362-920, 385362-901-33, 385362-6050-33, 385362-442-33, 385362-125-33, 385362-124-33 1 more385364-684-33, 385364-616-33, 385364-242-33, 222903-819-26, | 2019 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| SHENZHEN LYA SILICONE RUBBER PRODUCTS CO.,LTDFDA reg. 3008381928 | Shenzhen Guangdong, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10062058). 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.