# Anqing Clean Dental Instrument Technology Co.,Ltd (manufacturer, Anqing City Anhui, CN): 47 new FDA device listings, incl. probe, periodontic

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Anqing Clean Dental Instrument Technology Co.,Ltd |
| Role | Manufacturer |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device |
| Location | Anqing City Anhui, CN |
| New listings | 47 |
| Devices | Probe, Periodontic; Syringe, Periodontic, Endodontic, Irrigating; Accessories, Retractor, Dental; Forceps, Tooth Extractor, Surgical; Unit, Syringe, Air And/Or Water; Wax, Dental, Intraoral; Bedding, Disposable, Medical; Tray, Impression, Preformed; Bottle, Hot/Cold Water; Bandage, Cast |
| Product codes | EIX, EIC, EIF, EMG, ECB, EGD, KME, EHY, FPF, ITG, EJR, KXF, EKN, EKM, EJQ |
| Device classes | Class I, Class II |
| Medical specialties | Dental, General Hospital, Physical Medicine, General, Plastic Surgery, Pathology, Ophthalmic |
| Brand names | MIRROR, MOUTH (disposable dental mouth mirror/ handpiece mirror); disposable dental irrigation needles/ dental needle/ dental syringe; Pre Bent Needle Tips, Mixing Tips, irrigation syringe; Air Water Syringe Tips; disposable dental probe; UNIT, SYRINGE, AIR AND/OR WATER; Orthodontic wax, chwey; BEDDING, DISPOSABLE,MEDICAL |
| First new listing | 2026-06-03 |
| Latest new listing | 2026-07-21 |
| FDA registration number | 3038191347 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- 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: 2026-11-04T21:52:36.524Z.
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.