FDA product code EZZ: Prosthesis, Vas Deferens
EZZ is the FDA product code for prosthesis, vas deferens. It is a Class III device, reviewed by the Gastroenterology and Urology panel. FDA has cleared 1 510(k) submission under EZZ. The average 510(k) review took 68 days (median 68).
Classification
| Field | Value |
|---|---|
| Device name | Prosthesis, Vas Deferens |
| Device class | Class III |
| Review panel | GU — Gastroenterology and Urology |
| Medical specialty | Unknown |
| Premarket route | PMA |
| Implant | Yes |
Compare with all 510(k) review times · Search every EZZ clearance
Top EZZ applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Artiberia | 1 | 1985-07-02 |
Most recent EZZ clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K851719 | Artiberia | 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS | 1985-07-02 | 68 |
Recalls for EZZ devices
openFDA lists no recalls for product code EZZ.
Frequently asked questions
What is FDA product code EZZ?
EZZ is the FDA product code for prosthesis, vas deferens. It is a Class III device, reviewed by the Gastroenterology and Urology panel.
What device class is EZZ?
Class III. Typical premarket route: PMA.
How long does a 510(k) take for product code EZZ?
Across 1 cleared submissions the average was 68 days from receipt to decision (median 68).
Which companies have the most EZZ clearances?
Artiberia (1).
Next steps
- Run an FDA pathway report with predicate devices for product code EZZ
- Run a recall and safety report across every EZZ manufacturer
- Watch product code EZZ for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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