# Puli Healthcare (Thailand) Co., Ltd. (manufacturer, Bangkok Samut Prakan, TH): 29 new FDA device listings, incl. mask, oxygen

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Puli Healthcare (Thailand) Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device |
| Location | Bangkok Samut Prakan, TH |
| New listings | 29 |
| Devices | Mask, Oxygen; Forceps, General & Plastic Surgery; Finger Cot; Dressing, Wound, Hydrogel Without Drug And/Or Biologic; Dressing, Wound, Hydrophilic; Sling, Arm; Mirror, Mouth; Handle, Scalpel; Needle, Acupuncture, Single Use; Bandage, Elastic |
| Product codes | BYG, GEN, LZB, NAE, NAC, ILI, EAX, GDZ, MQX, FQM, GEC, ITG, OHO, KDC, HMP |
| Device classes | Class I, Class II |
| Medical specialties | Anesthesiology, General, Plastic Surgery, General Hospital, Physical Medicine, Dental |
| Brand names | CPR Face Shield; Tweezers; Finger Cot; Burn Gel Packets, Hydrogel dressing, hydrocolloid dressing, Chest seal; Combine Dressing, Trauma Bandage; Calcium Alginate Wound Dressings, Carbon Fiber Wound Dressings, Chitin Wound Dressings, Wound Pad; Triangular Bandage; Disposable dental mirror |
| First new listing | 2026-06-02 |
| Latest new listing | 2026-06-02 |
| FDA registration number | 3045742729 |
| 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.