Preat

Preat Corporation · Model 1500632 · UDI-DI 00842092169186

EGG Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

O-Ring Overdenture Complete #2 w/housing;. kit contains . 3 O-Ring Black Rings #2 Micro Single . 1 O-Ring Overdenture Analog #2 Micro . 1 O-Ring Castable Male #2 Micro . 1 O-Ring Metal Retainer #2 & 2M . 1 O-Ring Yellow Processing #2 Micro Single

Recalls

Date	Firm	Reason
2008-01-10	Straumann Usa, Llc	Mislabeled package: Narrow Connection (NC) Closure Screws contain closure screws for the regular connection (RC) bone level implant. The RC closures screw is larger (3.5mm diamete

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.