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PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDBP-040-2 Product Usage: -The PDBP-001 Battery is a single use (non-rechargeable) sterile lithium ion battery accessory that powers the PDSD Surgical driver. There is only one PDSD Surgical driver currently being produced (PDSD-5000) and the battery only works to power this driver. -The PDSD Series surgical drivers are Pro-Dex Branded surgical fixation drivers meant to drive surgical screws into bone in the CMF region of the body. They are class I exempt (Product codes GEY/GXL) battery powered hand pieces with a fixed collet. The only accessory is the PDBP-001 battery.

FDA Enforcement
Class II ·Terminated·Pro-Dex Inc·August 28, 2019

DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

SOZO Bilateral Arm L-Dex Software

FDA Enforcement
Class II ·Ongoing·Impedimed Limited·November 1, 2023

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S

FDA Enforcement
Class II ·Ongoing·Katalyst Surgical, LLC·May 13, 2026

VIDAS DEX@, Dimer Exclusion II, REF 30455-01

FDA Enforcement
Class II ·Ongoing·bioMerieux, Inc.·January 5, 2022

Thio Med w/Dex, Hem, Vit K (7ml) 20/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

FDA Enforcement
Class II ·Terminated·Remel Inc·May 29, 2019

Thio Med w/o Ind, w/Dex (18ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

FDA Enforcement
Class II ·Terminated·Remel Inc·May 29, 2019

Thio Med w/Dex, Hem, Vit, K (7ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

FDA Enforcement
Class II ·Terminated·Remel Inc·May 29, 2019

Thio Med w/o Ind, w/Dex (18ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

FDA Enforcement
Class II ·Terminated·Remel Inc·May 29, 2019

Thio Med w/Dex, Hem, Vit K (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

FDA Enforcement
Class II ·Terminated·Remel Inc·May 29, 2019