# Ad Supply Group Limited (foreign exporter, London London, City of, GB): 39 new FDA device listings, incl. drills, burrs, trephines & accessories (simple, powered)

**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 | 39 |
| Devices | Drills, Burrs, Trephines & Accessories (Simple, Powered); Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece; Bone Mill; Incubator, Neonatal; Condenser, Heat And Moisture (Artificial Nose); Oximeter; Analyzer, Gas, Sevoflurane, Gaseous-Phase (Anesthetic Concentration); Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration); Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.); Analyzer, Gas, Isoflurane, Gaseous-Phase (Anesthetic Concentration) |
| Product codes | HBE, ERL, LYS, FMZ, BYD, DQA, NHP, CBQ, CBR, NHQ, CBS, CCK, NHO, FOZ, FRC |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Neurology, Ear, Nose, Throat, Orthopedic, General Hospital, Anesthesiology, Cardiovascular, Hematology, General, Plastic Surgery, Clinical Chemistry, Radiology, Obstetrics/Gynecology, Gastroenterology, Urology |
| Brand names | System, imaging, pulsed echo, ultrasonic; Clamp, umbilical; Clip, implantable |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-10-13 |
| 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.