30 results · 21ms · Sources: EU EUDAMED, US FDA

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HEMOSIL RECOMBIPLASTIN 2G

FDA 510(k)
FDA Class 2 ·Hematology

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481110719·LOCATOR R-Tx Abutment for 3.6mm EV Internal Con...

LOCATOR, Dentsply Sirona System

FDA UDI
Zest Anchors, LLC·00840481131622·LOCATOR R-Tx Attachment System for Abutment EV ...

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690040·Advanced Dental Implant Ø4.2mm L6mm

LOCATOR R-Tx, Dentsply Sirona System

FDA UDI
Zest Anchors, LLC·00840481137044·LOCATOR R-Tx Abutment EV (S) 5mm

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481115004·LOCATOR F-Tx Abutment for 3.6mm EV Internal Con...

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690255·Titanium Angulated Abutment Internal Hex. Knife...

General Instrument

FDA UDI
ORTHOPEDIATRICS CORP.·00841132127063·Locking Plier

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481129124·LOCATOR R-Tx Abutment, 3.6mm Astra EV Connectio...

Scwire

FDA UDI
ORTHOPEDIATRICS CORP.·00841132123966·2.5 Compression Nut

Barrier, Adhesion, Cardiovascular

FDA Pre-Market Approval
FDA Class 3 ·REPEL-CV BIORESORBABLE ADHESION BARRIER

CYNOSURE PHOTOGENICA DL

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

IMMULITE VALPROIC ACID, IMMULITE 2000 VALPROIC ACID, CATALOG # LKVA1, LKVA5 & L2KVA2, L2KVA6

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

Barrier, Adhesion, Cardiovascular

FDA Pre-Market Approval
FDA Class 3 ·REPEL-CV BIORESORBABLE ADHESION BARRIER

Barrier, Adhesion, Cardiovascular

FDA Pre-Market Approval
FDA Class 3 ·REPEL-CV

PLICATOR

FDA Adverse Event
Injury ·NDO SURGICAL, INC.·Product code KOG·December 4, 2007

ASR XL TAP SLV ADAP 12/14+2

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 22, 2013

ARCHITECT I2000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·April 26, 2011

PULSE GEN MODEL 102

FDA Adverse Event
Malfunction ·CYBERONICS, INC.·Product code MUZ·July 2, 2008

REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly

FDA Recall
Open, Classified ·Stryker Sustainability Solutions·Product code KCY·May 31, 2024