# Shenzhen Jpy Ion-Tech. Co., Ltd. (contract sterilizer, Shenzhen Guangdong, CN): 37 new FDA device listings, incl. dressing, wound, hydrophilic

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Shenzhen Jpy Ion-Tech. Co., Ltd. |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Shenzhen Guangdong, CN |
| New listings | 37 |
| Devices | Dressing, Wound, Hydrophilic; Dressing, Wound, Drug; Dressing, Wound, Occlusive; Wound Dressing With Animal-Derived Material(S); Electrosurgical, Cutting & Coagulation & Accessories; Bandage, Liquid; Labware, Assisted Reproduction; Electrocautery, Gynecologic (And Accessories); Hemostatic Wound Dressing Without Thrombin Or Other Biologics; Labware, Assisted Reproduction, Exempt |
| Product codes | NAC, FRO, NAD, KGN, GEI, KMF, MQK, HGI, QSY, PUD, OHW, ORZ, KBN, GCJ, EMX |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General, Plastic Surgery, General Hospital, Obstetrics/Gynecology, Ophthalmic, Ear, Nose, Throat, Gastroenterology, Urology |
| Brand names | foam dressing; LUOFUCON HyperSorb Hydrofiber Wound Pad; Maxorb II Alginate; LUOFUCON Alginate Dressing; Qwick wound dressing; EQUOS Alginate; EQUOS Ag; Maxorb II Ag |
| First new listing | 2026-05-08 |
| Latest new listing | 2026-08-27 |
| FDA registration number | 8043396 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- 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: 2026-10-28T20:51:27.468Z.
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.