VIBE Technologies
Greeley, CO
VIBE Technologies appears in FDA device records in Greeley, CO. FDA records list no 510(k) clearances, no PMA records and no registered establishments. As of , FDA records show 2 recalls for this company.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 2
- Registered establishments
- 0
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
No FDA product codes recorded against this company.
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-0582-2009 | QuantumPulse machine. Vibe Technologies, Greeley, CO. The device is used to create light wave frequencies to effect cellular activity. | Medical device marketed without marketing approval for claims that include strengthening, recharging and removing toxins from cells. | Terminated | ||
| Z-0201-2009 | Vibe Technologies, VIBE machine, Vibrational Integrated Biophotonic Energizer. | Medical device marketed without marketing approval for claims that include cures cancer, infections, depression. | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain