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Sign in to claim this brandInrad
US
Last updated May 27, 2026
Information
- Country
- US
- Address
- —
- Website
- inradinc.com
- —
- —
- [email protected]
- Phone
- 6163017800
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 940023385
Catalogue (78)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Inrad | 681020 | FDA UDI | Class II | Active |
| Inrad | 991016 | FDA UDI | Class II | Active |
| Inrad | 671018 | FDA UDI | Class II | Active |
| Inrad | 54622 | FDA UDI | Class II | Active |
| Inrad | 691516 | FDA UDI | Class I | Active |
| Inrad | 670514 | FDA UDI | Class II | Active |
| Inrad | 57018 | FDA UDI | Class II | Active |
| Inrad | 55019 | FDA UDI | Class II | Active |
| Inrad | 991014 | FDA UDI | Class II | Active |
| Inrad | 601615 | FDA UDI | Class II | Active |
| Inrad | 602009 | FDA UDI | Class II | Active |
| Inrad | 670518 | FDA UDI | Class II | Active |
| Inrad | 40050 | FDA UDI | Class II | Active |
| Elitecore Full Core Biopsy Device 18gax10cm, 18gax15cm, 18gax20, With/Hilitier 18gax10cm , W/Hiliter 18gax15cm | K112945 | FDA 510(k) | Class II | Active |
| Revolution Full Core Biopsy | K090611 | FDA 510(k) | Class II | Active |
| Precisecore 10 Mm Biopsy Device- 14ga X 5 Cm Model 670514, 671014, 670518 671018, 670520 | K093399 | FDA 510(k) | Class II | Active |
| Ultraclip Ii Us | K042341 | FDA 510(k) | Class II | Active |
| Ultraclip Ii Mr | K041201 | FDA 510(k) | Class II | Active |
| Selectcore Variable Throw Biopsy Device Model 991014, 991514, 991018, 991518, 992018 | K093256 | FDA 510(k) | Class II | Active |
| Trilogy Tissue Marker | K240429 | FDA 510(k) | Class II | Active |
| C0-Axial Introducer Needle | K981721 | FDA 510(k) | Class II | Active |
| Accucore Core Biopsy Needle Catalog Codes:581014, 581614, 581618, 582018, 582518, 581620, 582020, 581214 | K981166 | FDA 510(k) | Class II | Active |
| ExpressCore Biopsy Device | K243886 | FDA 510(k) | Class II | Active |
| EasyMark Tissue Marker | K183503 | FDA 510(k) | Class II | Active |
| Ultraclip Tissue Marker | K993785 | FDA 510(k) | Class II | Active |
| Accucore Single Action Core Biopsy Device | K000612 | FDA 510(k) | Class II | Active |
| Iv Decanter-Flexible | K980587 | FDA 510(k) | Class II | Active |
| Ultraclip Ii Wing And Ultraclip Ii Coil | K063238 | FDA 510(k) | Class II | 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 |
|---|---|---|---|---|
| Dec 20, 2010 | Z-1063-2011 | — | terminated | This lot of product has the wrong expiration date on the carton label. The pouches contained the correct expiration date. |