231 results
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57ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VENES HIGH COMPRESSION MEDICAL STOCK-
FDA 510(k)
FDA Class 2
·General Hospital
ELVAREX CCL 2, KNEE HIGH, OPEN TOE, COLOR BLUE
FDA Adverse Event
Other
·Product code DWL·June 29, 2012
BOSSONG HOSIERY MEDICAL COMPRESSION STOCKINGS 8-15 MMHG, BOSSONG HOSIERY ANTI-EMBOLISM STOCKINGS 10-20 MMHG, BOSSONG HOS
FDA 510(k)
FDA Class 2
·General Hospital
JOBST MEDICAL COMPRESSION STOCKING 15-20 MMHG SIZE MEDIUM CAT NO. 119179, BLACK
FDA Adverse Event
Injury
·BSN MEDICAL, INC.·Product code LLK·August 9, 2018
JUZO DYNAMIC COMPRESSION STOCKING, OPEN TOE 3511 TYPE AD SIZE IV 5CMSILICONE
FDA Adverse Event
Injury
·JULIUS ZORN, INC.·Product code FQL·August 17, 2022
CURAD SIZE D COMPRESSION STOCKINGS
FDA Adverse Event
UNK·Product code FQL·January 7, 2019
Truform Therapeutic Classic Medical Style Compression Stockings 20-30 mmHG, Truform Therapeutic Classic Medical Style Compression Stockings 30-40 mmHG, A Div of SAI, Cincinnati, OH 45209 Product Usage: To help relieve tired, heavy legs, and moderate to pronounced varicose veins and swelling.
FDA Recall
Terminated
·Surgical Appliance Industries·Product code FQL·October 7, 2011
SIGVARIS COMPRESSION PANTYHOSE
FDA Adverse Event
Injury
·SIGVARIS, INC.·Product code FQL·August 14, 2025
JUZO COMPRESSION PANTYHOSE
FDA Adverse Event
Injury
·JULIUS ZORN, INC.·Product code FQL·August 14, 2025
OB PACK
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, LP·Product code OKV·June 2, 2025
ARROW HEMODIALYSIS KIT: 2-L 15 FR X 19 CM
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code MSD·October 28, 2025
COMFORT WEAR
FDA Adverse Event
Death
·THE MARENA GROUP, INC.·Product code MDR·March 26, 2003
SYNVISC ONE
FDA Adverse Event
Injury
·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·March 6, 2019
OB PACK
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, LP·Product code OKV·May 27, 2025
TRIATHLON CR FEM COMP #4 R-CEM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·December 21, 2018
VNUS CLOSURE
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code GEI·November 3, 2025
BASEPLATE
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWS·October 14, 2014
BASEPLATE
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWS·November 20, 2014
SMR SYSTEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code PHX·May 17, 2023
6.5MM CENTER SCREW - 28MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWS·November 20, 2014