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Sign in to claim this brandSUMMIT INDUSTRIES, LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 7555 N. Caldwell Avenue, Niles, IL, 60714
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1450503
- DUNS Number
- —
Catalogue (32)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Summit | A-172F | FDA UDI | Class I | Active |
| Summit | S203 | FDA UDI | Class I | Active |
| Summit Radiographic table | S211 | FDA UDI | Class II | Active |
| Summit | S225 | FDA UDI | Class I | Active |
| Summit Radiographic table | C256 | FDA UDI | Class II | Active |
| Summit | S111 | FDA UDI | Class I | Active |
| Summit | J700 | FDA UDI | Class I | Active |
| Summit | S102 | FDA UDI | Class I | Active |
| Summit Radiographic Mobile Table | ST1000 | FDA UDI | Class II | Active |
| Summit | S114 | FDA UDI | Class I | Active |
| Summit Radiographic table | S223 | FDA UDI | Class II | Active |
| Summit | S108 | FDA UDI | Class I | Active |
| Summit Radiographic table | S210 | FDA UDI | Class II | Active |
| Summit | SST-3001-RS | FDA UDI | Class I | Active |
| Summit | S109 | FDA UDI | Class I | Active |
| Summit | S105 | FDA UDI | Class I | Active |
| Summit X-ray Collimator | D800 | FDA UDI | Class II | Unknown |
| Summit Radiographic table | S222 | FDA UDI | Class II | Active |
| Summit | S107 | FDA UDI | Class I | Active |
| Summit | S113 | FDA UDI | Class I | Active |
| Summit Radiographic table | S204 | FDA UDI | Class II | Unknown |
| Summit Radiographic table | S212 | FDA UDI | Class II | Active |
| Summit Radiographic table | S200 | FDA UDI | Class II | Active |
| Summit | J1000 | FDA UDI | Class I | Active |
| Amrad Medical OTS Digital Radiography System, Amrad Medical DFMTS Digital Radiography SystemAmrad Medical FRS Digital Radiography System, | K153119 | FDA 510(k) | Class II | Active |
| C900 X-Ray Film Processor | K874908 | FDA 510(k) | Class II | Active |
| Rdiographic Wall Holder Or Film Receptor | K851440 | FDA 510(k) | Class I | Active |
| Xma 325 (x-Ray Generator) | K850117 | FDA 510(k) | Class I | Active |
| Floor To Wall Or Floor To Ceiling Tubestand;radiog | K850198 | FDA 510(k) | Class I | Active |
| Xma Integrated Table | K850118 | FDA 510(k) | Class II | Active |
| Colli-Matetm Model No. B800 | K874687 | FDA 510(k) | Class II | Active |
| Amrad Medical AAU Digital Radiography System; Amrad Medical AAU Plus Digital Radiography System; Amrad Medical DFMT Digital Radiography System; Amrad Medical FMT Digital Radiography System | K173823 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (4)
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 28, 2014 | Z-0468-2015 | — | terminated | The welds on J700 tube stands may be insufficient resulting in tube stand breakage, damage to the X-Ray machine, and/or patient or healthcare provider injury. |
| Aug 10, 2007 | Z-1216-2007 | — | terminated | The D800 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table. |
| Aug 10, 2007 | Z-1217-2007 | — | terminated | The E600 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table. |
| Aug 10, 2007 | Z-1218-2007 | — | terminated | The F100 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table. |