25 results
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22ms
·
Sources: EU EUDAMED, US FDA
OptiMap Catheter - 60mm (OPTI-CATH2-60)
FDA 510(k)
FDA Class 2
·Cardiovascular
delto-pectoral cutting guide
FDA UDI
FOURNITURES HOSPITALIERES INDUSTRIE·03661489610127·
10PW - Oklahoma Gas & Electric - Poly White
FDA UDI
Certified Safety Manufacturing, Inc.·00766588210124·10PW - Oklahoma Gas & Electric - Poly White
Humelock Cemented Shoulder Prosthesis
FDA UDI
FX SOLUTIONS·03701037303603·TRIAL OFFSET HEAD 39x15
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515036970·Lempert Rongeur, 2mm bite, str, 7 1/2"
Silverstone Interbody Fusion System
FDA UDI
Altus Spine, LLC·B417PS2610121·PEEK, TLIF, 26L X 10W X 12H
Symmetry Miller
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482062708·Symmetry® Rasp, Miller Bone, Double-Ended, 5 mm...
SKYHAWK
FDA UDI
Orthofix US LLC·18257200094738·CURETTE - STRAIGHT #1
TLS 5.0
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030CX2610120·Interbody Fusion Device 7DEG x 26L x 10W x 12H
Savant Lumbar Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C31426101200·Titanium PLIF Spacer, 26 x 10 x 12mm, 0 deg
Savant Lumbar Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C30426101280·PEEK PLIF Spacer, 26 x 10 x 12mm, 8 deg
Savant Lumbar Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C30426101200·PEEK PLIF Spacer, 26 x 10 x 12mm, 0 deg
Savant Lumbar Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C3242610120CT0·PEEK PLIF Spacer with Titanium Plasma Coating, ...
Savant Lumbar Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C3242610128CT0·PEEK PLIF Spacer with Titanium Plasma Coating, ...
Savant Lumbar Interbody Fusion System
FDA UDI
CURITEVA, INC.·B648C31426101280·Titanium PLIF Spacer, 26 x 10 x 12mm, 8 deg
Easy-Load Lens Delivery System
FDA 510(k)
FDA Class 1
·Ophthalmic
AXSOS PLUS LOCKING PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 17, 2025
HNM Medical
FDA UDI
HNM STAINLESS, LLC.·00842962115367·MILLER BONE RASPATORY, 7 1/4", DOUBLE ENDED, 5M...
PEN NDL 32G 4MM PRO 100 BOX 1200 US
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·August 21, 2025