FDA Device Intelligence
Home › Stille AB › STILLE Elevators

STILLE Elevators

Stille AB · Model 111-22569-18 · UDI-DI 07332339212445

HTE
0
510(k) clearances
137
Adverse events (1 deaths)
3
Recalls
175
Facilities

Description

BONE LEVER HOHMANN STILLE flat 18 mm 25.5 cm 10 in

Recalls

DateFirmReason
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.

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.