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Sign in to claim this brandMILESTONE SCIENTIFIC, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 425 Eagle Rock Ave., Roseland, NJ, 07068
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
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- FDA FEI Number
- 3004082685
- DUNS Number
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Catalogue (53)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| the Wand Handpiece | WA-2050-305 | FDA UDI | Class II | Active |
| Epidural Disposable Kit | EPI-6010 | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040 SAF-305 | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050A | FDA UDI | Class II | Active |
| CompuFlo Epidural | EPI-6000-110 | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040 SAF-2725 | FDA UDI | Class II | Active |
| Epidural Disposable Box | EPI-6100-01 | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040ASAF | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040 SAF-2725 | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040 SAF-305 | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040 SAF-301 | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050-301 | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050-305 | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050-301 | FDA UDI | Class II | Active |
| Epidural Disposable Kit | EPI-6011 | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050A | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040 SAF-2725 | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040ASAF | FDA UDI | Class II | Active |
| CathCheck Disposable Kit | EPI-6011-03 | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040 SAF-305 | FDA UDI | Class II | Active |
| CathCheck Disposable Kit | EPI-6100-03 | FDA UDI | Class II | Active |
| CompuFlo Epidural Computer Controlled Anesthesia System | EPI-6000-110 | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050A | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040 SAF-301 | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040 SAF-301 | FDA UDI | Class II | Active |
| Safety Wand STA Handpiece | STA-5040ASAF | FDA UDI | Class II | Active |
| CathCheck Disposable Kit (Pre-assembled) | EPI-6010-03 | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050-2725 | FDA UDI | Class II | Active |
| CompuFlo Epidural Trainer 110V/220V | EPI-6500T | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050-2725 | FDA UDI | Class II | Active |
| CompuFlo Epidural Computer Controlled Anesthesia System | EPI-6000-220 | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050-2725 | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040 SAF-2725 | FDA UDI | Class II | Active |
| Epidural Disposable Kit | EPI-6010-01 | FDA UDI | Class II | Active |
| Safety Wand Handpiece | WA-2040ASAF | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050A | FDA UDI | Class II | Active |
| Epidural Trainer Disposable Kit | EPI-6510T | FDA UDI | Class II | Active |
| SAFETY WAND Handpiece | WA-2040 SAF-301 | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050-301 | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050-301 | FDA UDI | Class II | Active |
| Saftey Wand STA Handpiece | STA-5040 SAF-305 | FDA UDI | Class II | Active |
| Epidural Disposable Kit | EPI-6100 | FDA UDI | Class II | Active |
| CathCheck Disposable Kit | EPI-6010-5 | FDA UDI | N/A | Unknown |
| CathCheck Disposable Kit | EPI-6100-5 | FDA UDI | N/A | Unknown |
| the Wand STA Handpiece | STA-5050-305 | FDA UDI | Class II | Active |
| CompuDent STA Drive Unit | STA-5220 | FDA UDI | Class II | Active |
| the Wand Handpiece | WA-2050-2725 | FDA UDI | Class II | Active |
| the Wand STA Handpiece | STA-5050-305 | FDA UDI | Class II | Active |
| CompuDent-STA™ Drive Unit | STA-5110 | FDA UDI | Class II | Active |
| Compuflo | K053554 | FDA 510(k) | Class II | Active |
Related Companies
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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 |
|---|---|---|---|---|
| Feb 11, 2015 | Z-1952-2015 | — | terminated | Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument. |