Histoware Prefilled Vials - non sterile

FDA registration

Protective Industries, Inc.·1 product·🇺🇸 United States

9 French, 120mm Lighted Suction Tube

FDA registration

KATALYST SURGICAL, LLC·2 products·🇺🇸 United States

Castroviejo Delicate Straight Needle Holder

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

ISOCLEAN IOL Cutter

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

iQ Curved ILM Forceps

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

Trabeculotome Set, left and right

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

Sapphire Crescent Knife, Straight Handle

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

AOC, OSTENE, AOC IMPLANT MATERIAL, CERETENE, OSTENE LUBE, AOC-LV

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

MX608WN5

FDA registration

PT. SUKSES ABADI INDONESIA·1 product·🇮🇩 Indonesia

Immunosuppressants Level 3

FDA UDI

UTAK LABORATORIES, INC.·B800416320·Immunosuppressants Level 3

Diode Laser Tips

FDA UDI

Biolase, Inc.·00647529000366·A single-use non-sterile fiberoptic laser tip i...

100 ml Bulb and JP Flat 3/4 fenestration 3 x 7 mm

FDA UDI

REDAX SPA·08034139290584·The drainage system is composed of a silicone r...

MTS

FDA UDI

MTS Medical UG (haftungsbeschränkt)·04260484573001·The LithoGold® is a compact mobile unit for ext...

AincA®

FDA UDI

ANESTHESIA ASSOCIATES, INC.·B005E13560·Mask, BOC Type, Inflatable Cuff Seal, 22mmF, Si...

AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Cocaine (COC) Rapid Test

Device

EU IVDD · Eu Ivd General ·Beijing Jinwofu Bioengineering Technology Co., Ltd.·On the market

Pronto doc - respiro facile

Device

EU MDR · Eu Md Class 1 ·Eurosirel Spa·On the market·32 countries

TOWER DOC Decompression Table

Device

EU MDD · Eu Md Class 2a ·Pivotal Health Solutions·On the market·16 countries

DIGITAL DOC

FDA 510(k)

FDA Class 1 ·Dental

DOC'S PROPLUGS EAR PLUGS

FDA 510(k)

FDA Unclassified ·Unknown