# Wenzhou Baiyu Glasses Technology Co.,Ltd (contract manufacturer, Wenzhou Zhejiang, CN): 6 new FDA device listings, incl. dressing, wound, hydrogel without drug and/or biologic

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Wenzhou Baiyu Glasses Technology Co.,Ltd |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer); Export Device to the United States But Perform No Other Operation on Device |
| Location | Wenzhou Zhejiang, CN |
| New listings | 6 |
| Devices | Dressing, Wound, Hydrogel Without Drug And/Or Biologic; Kit, Surgical Instrument, Disposable; Syringe, Antistick; Pack, Hot Or Cold, Disposable; Lubricant, Personal; Dressing, Wound, Hydrophilic |
| Product codes | NAE, KDD, MEG, IMD, NUC, NAC |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, General Hospital, Physical Medicine, Obstetrics/Gynecology |
| Brand names | DRMITSUI SODIUM HYALURONATE EYE DROPS; skin tag remover kit; QIDILA 1ml/cc Disposable Syringe with 30G 1/2" (12.7mm) Needle; FluMisch 1cc U-100 Syringes with 5/16"(8mm) 31 Gauge Needle; QIDILA 1ml/cc Disposable Syringe with 31G 1/4" (6mm) Needle; YVTYVT U-100 0.5ml/cc Syringe with 30G 5/16" (8mm) Needle; HKKA BALANCE PATCH; DRMITSUI VAGINAL PROBIOTICS GEL |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-07-12 |
| FDA registration number | 3038220293 |
| 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.