FDA product code POZ: Biopsy Needle Kit

POZ is the FDA product code for biopsy needle kit. It is a Class II device, regulated under 21 CFR 876.1075 and reviewed by the Gastroenterology and Urology panel. Devices under POZ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. FDA has posted 1 recall for POZ devices, 1 initiated in the last five years.

Definition

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Classification

Recalls for POZ devices

1 product recalls in 1 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2026-04-21.

Frequently asked questions

What is FDA product code POZ?

POZ is the FDA product code for biopsy needle kit. It is a Class II device, regulated under 21 CFR 876.1075 and reviewed by the Gastroenterology and Urology panel.

What device class is POZ?

Class II, regulation 21 CFR 876.1075. Typical premarket route: 510(k) exempt.

Have POZ devices been recalled?

Yes: 1 product recalls across 1 recall events; the most recent began 2026-04-21.

Next steps

• Run an FDA pathway report with predicate devices for product code POZ
• Run a recall and safety report across every POZ manufacturer
• Watch product code POZ 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.

All Gastroenterology and Urology product codes · FDA product code lookup · 510(k) database search · 510(k) review times