Home › KATENA PRODUCTS, INC. › Trab. Punch
Trab. Punch
KATENA PRODUCTS, INC. · Model K2-9506 · UDI-DI 00841668101995
HNJ
Prescription
3
510(k) clearances
12
Adverse events
1
Recalls
78
Facilities
Description
REPLACEMENT HEAD SET FOR K 2-9505
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-06-27 | Insight Instruments, Inc. | The product was registered and distributed as a Class I medical device and was subsequently determined to be a Class II medical device which requires FDA market clearance. |
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.