7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
×
SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-24928
FDA Enforcement
Class II
·Terminated·OMNIlife science Inc.·February 3, 2021
SERF Novae Dual Mobility Cup Insert 47/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-24728
FDA Enforcement
Class II
·Terminated·OMNIlife science Inc.·February 3, 2021
SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-25128
FDA Enforcement
Class II
·Terminated·OMNIlife science Inc.·February 3, 2021
SoftPerm (synergicon A) Daily Wear Contact Lenses, Rx Only, Sterile. Contents: One sterile contact lens, rigid center/soft hydrophilic skirt (25% water), in normal saline solution buffered with sodium bicarbonate. Ciba Vision Group, Duluth GA 30097 USA SoftPerm contact lenses are indicted for daily wear (class II device) for correction of visual accuracy for keratoconus and in non-aphakic persons with non-diseased eyes that are myopic or hyperopic
FDA Recall
Terminated
·CIBA Vision Puerto Rico, Inc. El Jibaro·Product code LPL·February 1, 2011
SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-25128
FDA Recall
Terminated
·OMNIlife science Inc.·Product code LZO·December 21, 2020
SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-24928
FDA Recall
Terminated
·OMNIlife science Inc.·Product code LZO·December 21, 2020
SERF Novae Dual Mobility Cup Insert 47/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-24728
FDA Recall
Terminated
·OMNIlife science Inc.·Product code LZO·December 21, 2020