37 results · 26ms · Sources: EU EUDAMED, US FDA

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CLINICARD PHOSPHORUS

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

Posicast® Thermoplastic

FDA UDI
MEDTEC, INC.·10841439101480·PR3 Multiperfo mask

Ceramill® Zolid

FDA UDI
Amann Girrbach AG·E4947600301·

Washbon

FDA UDI
ORMCO CORPORATION·00889989043273·LOWER LEFT SECOND MOLAR WASHBON BAND SIZE 30

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600301·Mand. 2. Bicuspidband left 30

RIBFIX BLU SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00888233000178·

Daytona

FDA UDI
Seaspine Orthopedics Corporation·10889981130619·Ti Locking Cap Asm. 4.5mm, Small Stature

Retractor Blade

FDA UDI
KOROS U.S.A., INC.·10840199531476·22X65mm Deep 30 Degree Angled Titanium Shoulder...

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668110584·COAXIAL IRRIGAT-ASPIRAT TIP 45 DEG ASP

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600300101·Mand. 2. Bicuspidband left 30

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600300501·Mand. 2. Bicuspidband left 30

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600300051·Mand. 2. Bicuspidband left 30

TI LOCKING CAP ASM. 4.5MM SMALL STATURE

FDA Adverse Event
Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code NKB·September 3, 2024

TI LOCKING CAP ASM. 4.5MM SMALL STATURE

FDA Adverse Event
Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code NKB·September 3, 2024

CAST MATERIAL (WICKET STOCKINETTE)

FDA 510(k)
FDA Class 1 ·Physical Medicine

THE DOUBLE GLOVE

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

TI LOCKING CAP ASM. 4.5MM SMALL STATURE

FDA Adverse Event
Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code NKB·September 3, 2024

LOCKING BOLT MEASURING DEVICE F/TROCHANTERIC FIXATION NAILS

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTJ·April 16, 2020

COCR LOCKING CAP 4.5MM, SMALL STATURE, T25, BT

FDA Adverse Event
Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code NKB·September 3, 2024

COCR LOCKING CAP 4.5MM, SMALL STATURE, T25, BT

FDA Adverse Event
Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code NKB·September 3, 2024