FDA Device Intelligence
Home › SHIPPERT MEDICAL TECHNOLOGIES, INC › DENVER SPLINT

DENVER SPLINT

SHIPPERT MEDICAL TECHNOLOGIES, INC · Model 10-1500-05KL · UDI-DI 00893398002011

EPP
10
510(k) clearances
19
Adverse events
2
Recalls
38
Facilities

Recalls

DateFirmReason
2011-02-21Medtronic Xomed, Inc.Medtronic Xomed, Inc. Jacksonville, FL issued a recall on Feb 21, 2011 for all lots of the alcohol pad packaged with the Medtronic's External Nasal Splints REF 1528116 (sm), 152812
2011-02-21Medtronic Xomed, Inc.Medtronic Xomed, Inc. Jacksonville, FL issued a recall on Feb 21, 2011 for all lots of the alcohol pad packaged with the Medtronic's External Nasal Splints REF 1528116 (sm), 152812

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.