FDA Device Intelligence
Home › RZ-Medizintechnik GmbH › RZ Medizintechnik GmbH

RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 200-200-170 · UDI-DI 04049197097215

FTY Prescription
10
510(k) clearances
436
Adverse events
5
Recalls
403
Facilities

Description

Bone calipers, angled, blunt 180mm (7"), opening: 140mm

Recalls

DateFirmReason
2015-03-05SpineFrontier, Inc.The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle Screw System may be used incorrectly as the Surgical Technique does not adequately convey the intended use
2010-10-22Lemaitre Vascular, Inc.Box label (Top Part). Lot and Expiration Date information were switched.
2010-10-22Lemaitre Vascular, Inc.Box label (Top Part). Lot and Expiration Date information were switched.
2010-10-22Lemaitre Vascular, Inc.Box label (Top Part). Lot and Expiration Date information were switched.
2010-10-22Lemaitre Vascular, Inc.Box label (Top Part). Lot and Expiration Date information were switched.

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.