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Sign in to claim this brandQmed, Inc.
US
Last updated May 23, 2026
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Catalogue (81)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Restylane-L | Gel 1 mL Syringe | FDA UDI | Class III | Active |
| Restylane Eyelight | Gel 0.5 mL Syringe-Demo | FDA UDI | Class III | Active |
| Restylane Lyft with Lidocaine | Gel 1.0 ml syringe - demo | FDA UDI | Class III | Active |
| Restylane Contour | Gel 1 mL Syringe | FDA UDI | Class III | Active |
| Restylane Refyne | Gel 1.0 ml syringe | FDA UDI | Class III | Active |
| Restylane Refyne | Gel 1 mL Syringe-Demo | FDA UDI | Class III | Active |
| Restylane Refyne | Gel 1.0 ml syringe - demo | FDA UDI | Class III | Active |
| Restylane Kysse | Gel 1 mL Syringe-Demo | FDA UDI | Class III | Active |
| Restylane-L | Gel 1.0 ml syringe | FDA UDI | Class III | Unknown |
| Perlane-L | Gel 1.0 ml syringe | FDA UDI | Class III | Unknown |
| Restylane Silk | Gel 1.0 ml syringe - demo | FDA UDI | Class III | Active |
| Restylane-L | Gel 1.0 ml syringe | FDA UDI | Class III | Active |
| Restylane Defyne | Gel 1.0 ml syringe - demo | FDA UDI | Class III | Active |
| Restylane-L | Gel 1.0 ml syringe - demo | FDA UDI | Class III | Active |
| Sculptra | 1 vial pack-Sample | FDA UDI | Class III | Active |
| Restylane Lyft with Lidocaine | Gel 1 mL Syringe | FDA UDI | Class III | Active |
| Restylane Silk-L | 1.0 ml syringe | FDA UDI | Class III | Active |
| Restylane Silk-L | 1.0 ml syringe | FDA UDI | Class III | Unknown |
| Restylane Contour | Gel 1 mL Syringe - Demo | FDA UDI | Class III | Active |
| Restylane Lyft with Lidocaine | Gel 1 mL Syringe | FDA UDI | Class III | Active |
| Monitor One | K841172 | FDA 510(k) | Class II | Active |
| Interp-1000 | K921476 | FDA 510(k) | N/A | Active |
| Qmed Self Adhering Electrode | K862377 | FDA 510(k) | Class II | Active |
| A.r.m. (aspen Return Monitor) | K873591 | FDA 510(k) | Class II | Active |
| Qekg Electrocardiograph | K897121 | FDA 510(k) | Class II | Active |
| Q-Med Electrode | K840465 | FDA 510(k) | Class II | Active |
| Bicord By Qmed | K863091 | FDA 510(k) | Class II | Active |
| Monitor One Ndx | K972991 | FDA 510(k) | Class II | Active |
| Profilomat | K932109 | FDA 510(k) | Class II | Active |
| Qmed System 2150 | K861437 | FDA 510(k) | Class II | Active |
| Kleenit By Qmed | K843559 | FDA 510(k) | N/A | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 30, 2003 | Z-0246-04 | — | terminated | This wholesaler may have distributed some Prolene Mesh Counterfeit product with the Ethicon trademark. |