Veran Medical Technologies, Inc.
Nashville, TN, US
Veran Medical Technologies, Inc. appears in FDA device records in Nashville, TN. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Veran Medical Technologies, Inc. between 2006 and 2021. The busiest year on record is 2009, with 2. The most recent is 2021, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2006 | 1 |
| 2009 | 2 |
| 2010 | 1 |
| 2012 | 1 |
| 2017 | 1 |
| 2021 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K202346 | SPiN Vision Video Bronchoscope System | EOQ | Substantially Equivalent | |
| K170023 | SPiN Thoracic Navigation System | JAK | Substantially Equivalent | |
| K122106 | SPIN DRIVE ALWAYS-ON TIP TRACKED STEERABLE CATHETER ALWAYS-ON TIP TRACKED SHEATH ALWAYS-ON TIP TRACKED ASPIRATION NEEDLE | JAK | Substantially Equivalent | |
| K093995 | IG 4 IMAGE GUIDED SYSTEM | JAK | Substantially Equivalent | |
| K091934 | IG4 ENDOBRONCHIAL, MODEL SYS-0200, NAVIGATION GUIDEWIRE (ACCESSORY TO IG4 ENDOBRONCHIAL), MODEL INS-0300 | JAK | Substantially Equivalent | |
| K093146 | IG4 IMAGE GUIDED SYSTEM, MODEL: SYS-0200 | JAK | Substantially Equivalent | |
| K060903 | IG4 IMAGE GUIDED SYSTEM | JAK | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain