33 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Ergoline, Sun Angel, Soltron, Sundash and Palm Beach Tan Sunlamp Products
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SimPro™ Now
FDA UDI
Wellspect AB·07392532188978·Single Use Urinary Catheter with water sachet. ...
SimPro™ Now
FDA UDI
Wellspect AB·07333387032740·Single Use Urinary Catheter with water sachet. ...
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526814721·GENUMEDI PSS GREEN O
CoRoent
FDA UDI
Nuvasive, Inc.·00887517575395·CoRoent Ant TLIF Ti, 15x11x40mm 0°
CASTROVIEJO NEEDLE HOLDER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896017559·CASTROVIEJO NEEDLE HOLDER WITHOUT LOCK DELICATE...
ZB ProLift Narrow
FDA UDI
Life Spine, Inc.·00190837079277·
Malibu™
FDA UDI
Seaspine Orthopedics Corporation·10889981030131·PRECONTOURED ESS ROD, 5.5 x 400 mm
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702580068·E1/AG/SL-CT/NOP5-T-OH/CB
LOCKING COMPRESSION PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
DATEX-OHMEDA S/5 ANESTHESIA MONITOR WITH L-ANEO5 AND L-ANEO5A SOFTWARE, USING F-CU8 OR F-CU5(P) MONITOR FRAME OPTIONS
FDA 510(k)
FDA Class 2
·Cardiovascular
II Ring Retractor
FDA UDI
Automated Medical Products Corp.·00810118341342·Malleable Retractor 1" x 9" with Protective Edge
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·February 26, 2021
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·June 7, 2013
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·June 8, 2011
HOVEROUND CORPORATION
FDA Adverse Event
Injury
·HOVEROUND CORPORATION·Product code ITI·September 4, 2008
LOGIC CR TIB INSERT SLOPE++, SZ 3, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 5, 2024
LOGIC CR TIB INSERT STD, SZ 4, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 2, 2022
LOGIC CR TIB INSERT STD, SZ 1.5, 9 MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 10, 2025
LOGIC CR TIB INSERT SLOPE ++, SZ 3.5, 13 MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 18, 2024