17 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MHC Standard and NRFit Tip Syringes
FDA 510(k)
FDA Class 2
·General Hospital
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771012450·K-Wires, Single trocar, .035-inch (.9mm) diamet...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292688·
NA
FDA UDI
KEY SURGICAL, INC.·10849771049033·K-Wires, Single trocar, .035-inch (.9mm) diamet...
K-Wire w. trocar/round end 0.89mm/102mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM711310·K-Wire w. trocar/round end
0.89mm...
Novo Surgical Inc.
FDA UDI
NOVO SURGICAL, INC.·00842331132841·dressing forceps, standard pattern, serrated ha...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484221·K-Wire w. trocar/round end _x000D_...
FIDUCIAL MARKERS
FDA 510(k)
FDA Class 2
·Radiology
UNO
FDA 510(k)
FDA Class 2
·Dental
ISA CO2
FDA Adverse Event
Malfunction
·MASIMO - 15750 ALTON PKWY·Product code MWI·December 30, 2022
BD SYRINGE 30ML LL TIP CONV PAK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·October 15, 2024
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·June 14, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·July 11, 2011
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM
FDA Adverse Event
Injury
·BIOENTERICS CORP·Product code LTI·September 18, 2008
HAART 200 AORTIC ANNULOPLASTY RING
FDA Adverse Event
Injury
·CORCYM INC.·Product code KRH·May 8, 2025
HAART 200 AORTIC ANNULOPLASTY RING
FDA Adverse Event
Injury
·CORCYM INC.·Product code KRH·May 9, 2025
Exactech Equinoxe CAGE GLENOID, CEMENTED, alpha curvature, Mates with: a) 38, 41, 44 head, Small, Item Number 314-13-02, b) 38, 41, 44 head, Medium, Item Number 314-13-03, c) 38, 41, 44 head, Large, Item Number 314-13-04; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024