FDA Device Intelligence
HomeI.T.S. GmbH › Slotted Hammer

Slotted Hammer

I.T.S. GmbH · Model 1-1920 · UDI-DI 09120047308486

FZY
1
510(k) clearances
861
Adverse events
2
Recalls
266
Facilities

Description

Slotted Hammer

Recalls

DateFirmReason
2013-04-25SpineFrontier, Inc.Malfunction of slap hammer.
2008-05-07EBI, L.P.Customer complaint received regarding the separation of the mallet handle during a medical procedure.

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 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.