# Jm Medical Co., Ltd. (manufacturer, Liaocheng Shandong, CN): 8 new FDA device listings, incl. bandage, cast

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Jm Medical Co., Ltd. |
| Owner / operator | JM Medical Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device |
| Location | Liaocheng Shandong, CN |
| New listings | 8 |
| Devices | Bandage, Cast; Bag, Drainage, With Adhesive, Ostomy; Bag, Urine Collection, Leg, For External Use, Sterile; Sheath, Corrugated Rubber, For Non-Indwelling Catheter, Non-Sterile; Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use; Collector, Urine, (And Accessories) For Indwelling Catheter; Non-Surgical Gown; Dressing, Wound, Hydrogel Without Drug And/Or Biologic |
| Product codes | ITG, FON, FAQ, NNY, PYO, KNX, OEA, NAE |
| Device classes | Class I, Class II |
| Medical specialties | Physical Medicine, Gastroenterology, Urology, General Hospital, General, Plastic Surgery |
| Brand names | Healing bandage; ostomy bag; Urinary Leg Bag; Condom Catheter, External Catheter, Rusch Male Exeternal, Catheter; Medical tape; Ostomy remover spray; Isolation gown; Liquid protective dressing |
| First new listing | 2026-05-12 |
| Latest new listing | 2026-05-12 |
| FDA registration number | 3031582449 |
| 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.