2,580 results · 20ms · Sources: EU EUDAMED, US FDA

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Sterilucent HC 80TT Hydrogen Peroxide Sterilizer

FDA 510(k)
FDA Class 2 ·General Hospital

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481124570·LOCATOR R-Tx Attachment System, FairTwo S, Fair...

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690196532·AK3 4 in 1 A/P Cutting Block, size 5

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00841036032777·

N/A

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055001·MTM® NO TRACE (TM) 018 UL/4-4

IN-OVATION® L

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055011·IN-OVATION® L 018 UPPER 6-6

IN-OVATION® L

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055101·IN-OVATION® L 018 UL/7-7

Qualitative And Quantitative Hepatitis B Virus Antibody Assays

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe, PreciControl Anti-HBe

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197499767·Quervain Blade, curved 70x70m...

BRANEMARK INTEGRATION BIOHELIX IMPLANTS

FDA 510(k)
FDA Class 2 ·Dental

BD PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe, PreciControl Anti-HBe

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe

Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

FDA Pre-Market Approval
FDA Class 2 ·Elecsys Anti-HBe, PreciControl Anti-HBe

COLLEAGUE VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 8, 2008

APPLICATOR INNER SHAFT

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code LXH·June 26, 2013