Home › Preat Corporation › Preat
Preat
Preat Corporation · Model 3O694KS · UDI-DI 00842092173459
EGG
Prescription
10
510(k) clearances
3
Adverse events
1
Recalls
57
Facilities
Description
Ceka OL 694 KS Platirax (696 KS PL) (2-Pack); kit contains 2 Ceka OL 694 KS Platirax (696 KS PL) (Each) (3O694KS-1)
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 keyRead the docsData 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.
