# Turnxon Precision Co., Ltd (contract manufacturer, Dongguan Guangdong, CN): 3 new FDA device listings, incl. extractor

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Turnxon Precision Co., Ltd |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Dongguan Guangdong, CN |
| New listings | 3 |
| Devices | Extractor; Guide, Surgical, Instrument; Bit, Drill |
| Product codes | HWB, FZX, HTW |
| Device classes | Class I |
| Medical specialties | Orthopedic, General, Plastic Surgery |
| Brand names | 00-5978-020-00 FEMORAL PROVISIONAL EXTRACTOR; 00-5901-090-01 2 DEG VARUS RESECTION GUIDE; 00-5977-014-00 NEXGEN CEMENTED ST DRILL GDE; 00-5901-090-00 2 DEG VALGUS RESECTION GUIDE; 42-5399-018-14 PSN CEM TIB DRILL BIT 14X+30MM |
| First new listing | 2026-06-07 |
| Latest new listing | 2026-06-07 |
| FDA registration number | 3011534620 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.