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

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SUPRA SCAN DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Bur PM2-MIS P160 steel Ø2.0 St

FDA UDI
Bien-Air Surgery SA·17630055512083·

Sharps

FDA UDI
SHARPS COMPLIANCE CORP.·00634188001896·2-Gallon Sharps Container - Flexible Petal Lid

Oticon

FDA UDI
Oticon A/S·05707131163523·ACTO, RITE CBE

MINATURE HOHMANN ELEVATOR RETRACTOR

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896049505·MINATURE HOHMANN ELEVATOR RETRACTOR

simex

FDA UDI
SIMEX Medizintechnik GmbH·04052262385957·SIMEX cuff M suction

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001393·Invue Max, Three Level ACP, 78mm

N/A

FDA UDI
Doppkon GmbH & Co. KG·04262494462269·Hook Probe Square Handle Steel D 3.0mm, WL 260mm

RAEBBITT/EVOLUTION POWERED WHEELCHAIR

FDA 510(k)
FDA Class 2 ·Physical Medicine

MODIFIED STRAIGHT FIRE LASER FIBER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2024

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 21, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·February 23, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·October 7, 2025

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 13, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 20, 2025

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·June 11, 2024

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·March 6, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·April 20, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·December 8, 2023