# Ad Supply Group Limited (foreign exporter, London London, City of, GB): 40 new FDA device listings, incl. tube, laryngectomy

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Ad Supply Group Limited |
| Owner / operator | AD Supply Group Limited |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | London London, City of, GB |
| New listings | 40 |
| Devices | Tube, Laryngectomy; Electrosurgical, Cutting & Coagulation & Accessories; Instrument, Ultrasonic Surgical; Syringe, Antistick; Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase; Stain, Papanicolau; Catheter, Intravascular, Diagnostic; Cup, Prophylaxis; Tubes, Vials, Systems, Serum Separators, Blood Collection; Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
| Product codes | KAC, GEI, LFL, MEG, CCK, HZJ, DQO, EHK, JKA, FOZ, HBE, ERL, FRC, FMZ, ITX |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Ear, Nose, Throat, General, Plastic Surgery, General Hospital, Anesthesiology, Hematology, Cardiovascular, Dental, Clinical Chemistry, Neurology, Radiology, Gastroenterology, Urology, Obstetrics/Gynecology |
| Brand names | System, imaging, pulsed echo, ultrasonic; Clip, implantable; Clamp, umbilical |
| First new listing | 2026-05-13 |
| Latest new listing | 2026-10-23 |
| FDA registration number | 3030733800 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- Listed in the last 45 days.

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.