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Sign in to claim this brandESCALON MEDICAL CORP
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2440 SOUTH 179TH ST., NEW BERLIN, WI, 53146
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2183477
- DUNS Number
- —
Catalogue (23)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fiber Optic Light Guide | 45°Retinal Knife, Universal | FDA UDI | Class II | Active |
| Fiber Optic Light Guide | Wide Angle, 20 ga, Universal | FDA UDI | Class II | Active |
| Viscous Fluid Cannula | 9849-51 | FDA UDI | Class I | Active |
| Fiber Optic Light Guide | 45°, 20 ga, TREK/Greishaber | FDA UDI | Class II | Active |
| Fiber Optic Light Guide | Wide Angle, 20 ga, TREK/Greishabler | FDA UDI | Class II | Active |
| Fiber Optic Light Guide | DCR, 20 ga | FDA UDI | Class II | Active |
| Fiber Optic Light Guide | Iris Retractor, 20 ga | FDA UDI | Class I | Active |
| Fiber Optic Light Guide | Siepser Shielded | FDA UDI | Class II | Active |
| Irrigating Contact Lens | Minus | FDA UDI | Class I | Active |
| Fiber Optic Light Guide | 45°, 20 ga, Universal | FDA UDI | Class II | Active |
| Viscous Fluid Pack | 8170-11 | FDA UDI | Class II | Active |
| Fiber Optic Light Guide | 45° Retinal Knife, TREK/Greishaber | FDA UDI | Class II | Active |
| Universal Gas Mixing Kit | 9060-61 | FDA UDI | Class I | Active |
| Viscous Fluid Pack | 8170-51 | FDA UDI | Class II | Active |
| Fiber Optic Light Guide | Standard, 20 ga, TREK/Greishaber | FDA UDI | Class II | Active |
| ISPAN SF6 Intraocular Gas | 20 g Cylinder | FDA UDI | Class III | Active |
| Fiber Optic Light Guide | Standard, 20 ga, Universal | FDA UDI | Class II | Active |
| Irrigating Contact Lens | Flat | FDA UDI | Class I | Active |
| Fluid/Gas Tubing Set | 9006-11 | FDA UDI | Class II | Active |
| ISPAN C3F8 Intraocular Gas | 20 g Cylinder | FDA UDI | Class III | Active |
| Megavision Cpx, Megavision Fa, Model I And Ii | K002920 | FDA 510(k) | Class II | Active |
| Vascuview Tap Ultrasound System | K093613 | FDA 510(k) | Class II | Active |
| Vascuview Ultrasound System | K080049 | 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 |
|---|---|---|---|---|
| May 5, 2010 | Z-0132-2011 | — | terminated | The packaging of the vascular access device may potentially become damaged, compromising the sterility of the product. Use of a non-sterile product increases risk of patient infection. This recall involes: Model 78050 18 Gauge PD Access Vascular Access Device, Model 78060 Extended 18 Gauge PD Access Vascular Access Device, Model 75010 18 Gauge SmartNeedle Vascular Access Devices with Expiration Da |