Medi-Globe Corporation
7 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| EasyPass Guidewire (K153264) | Medi-Globe Corporation | 2016-05-19 |
| PolyCatch Retrieval Device (K142258) | Medi-Globe Corporation | 2014-09-30 |
| SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM (K133763) | Medi-Globe Corporation | 2014-05-15 |
| MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM (K091257) | Medi-Globe Corporation | 2009-05-08 |
| SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025 (K083802) | Medi-Globe Corporation | 2009-03-20 |
| SONOTIP II ULTRASOUND NEEDLE SYSTEM (K070129) | Medi-Globe Corporation | 2007-01-31 |
| MEDI-GLOBE ROTA-CUT SPHINCTEROTOME (K061684) | Medi-Globe Corporation | 2006-06-27 |
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Every clearance here is in the API, with alerts when new ones post.