10,000 results · 47ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SHARPOINT PDO (POLYDIOXANONE) SUTURES

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

WEGO-PDO Barbed Suture

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

PDS Barbed Suture, PDO MAXX Threads

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

PDO Max Suture with Dual Needle

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

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code NEW·April 1, 2010

NOVATHREADS

FDA Adverse Event
Injury ·ECTODERMA DBA COSMOFRANCE·Product code NEW·June 15, 2023

STRATAFIX SPIRAL

FDA Adverse Event
Injury ·SURGICAL SPECIALTIES CORPORATION·Product code NEW·April 14, 2025

SMUTH B

FDA Adverse Event
Injury ·PDO MAX·Product code NEW·December 29, 2025

PDO MAX SMOOTH THREAD

FDA Adverse Event
Injury ·PDO MAX·Product code NEW·December 4, 2025

PDO MAX THREADS LEVO AND SMUTH

FDA Adverse Event
Injury ·PDO MAX·Product code NEW·July 27, 2022

PDO THREAD

FDA Adverse Event
Injury ·PDO MAX·Product code NEW·January 12, 2025

Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)

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

DEMETECH POLYDIOXANONE SYNTHETIC MONOFILAMENT (PDO) ABSORBABLE SUTURE

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

PDO (POLYDIOXANONE) MONOFILAMENT SYNTHETIC ABSORBABLE SUTURE U.S.P.

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

CONTOUR THREAD SYNTHETIC ABSORBABLE PDO BARBED SUTURE

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

QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)

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

QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)

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

NOVATHREADS

FDA Adverse Event
Injury ·ECTODERMA DBA COSMOFRANCE·Product code NEW·May 26, 2023

NOVATHREADS

FDA Adverse Event
Injury ·ECTODERMA DBA COSMOFRANCE·Product code NEW·June 15, 2023

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 19, 2010