# Dongguan Quanding Medical Supplies Co., Ltd (manufacturer, Dongguan Guangdong, CN): 7 new FDA device listings, incl. unit, heating, powered

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Dongguan Quanding Medical Supplies Co., Ltd |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Dongguan Guangdong, CN |
| New listings | 7 |
| Devices | Unit, Heating, Powered; Set, Tubing And Support, Ventilator (W Harness); Bandage, Elastic; Cable, Electrode; Unit, Chilling; Pad, Heating, Powered; Irrigator, Powered Nasal |
| Product codes | IRQ, BZO, FQM, IKD, IMF, IRT, KMA |
| Device classes | Class I, Class II |
| Medical specialties | Physical Medicine, Anesthesiology, General Hospital, Ear, Nose, Throat |
| Brand names | Powered heating unit QD-CH101,QD-CH102,QD-CH103,QD-CH104,QD-CH105,QD-CH301,QD-CH302,QD-CH303,QD-CH304,QD-CH305; HT01,HT02,HT03,HT04,HT05,HT06,HT07,HT08,HCT01,HCT02,HCT03,HCT04,HCT05,HCT06,HCT07,HCT08; Ventilator Tubing QD-VT01,QD-VT02,QD-VT03,QD-VT04,QD-VT05,QD-VT06,QD-VT07,QD-VT08,QD-VT09,QD-VT10;CB-TB01,CB-TB02; CB-TB03,CB-TB04,CB-TB05,CB-TB06.; Fixed Strap or Accessory,QD-FA01,QD-FA02,QD-FA03,QD-FA04,QD-FA05,QD-FA06; CB-FS07,CB-FS08,CB-FS09,CB-FS10,CB-FS11,CB-FS12,CB-FS13,CB-FS14;CB-FS15.; QD-FA07,QD-FA08,QD-FA09,QD-FA10,QD-FA11,QD-FA12,QD-FA13,QD-FA14;QD-FA15;CB-FS01,CB-FS02,CB-FS03,CB-FS04,CB-FS05,CB-FS06; Electrode Cable QD-EC001,QD-EC002,QD-EC003,QD-EC004,QD-EC005,QD-EC006,QD-EC007,QD-EC008,QD-EC009 |
| First new listing | 2026-05-16 |
| Latest new listing | 2026-05-16 |
| FDA registration number | 3017450375 |
| 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.