LIQUIBAND FLEX

FDA registration

Sterigenics UK Limited·1 product·🇬🇧 United Kingdom

LIQUIBAND DUAL, MODEL LBD 001

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Tissue Adhesive For The Topical Approximation Of Skin

FDA classification

FDA Class 2 ·Tissue Adhesive For The Topical Approximation Of Skin

Redicare

FDA UDI

REDICARE LLC·B70901020760·First Aid Kit to aid in administering Cardiopul...

Oticon

FDA UDI

Oticon A/S·05707131164728·CHILI SP9, BTE 13 SP DBL DEMO

Panther TPS

FDA registration

PROWESS, INC.·1 product·🇺🇸 United States

CRYOMEGA

FDA registration

PREMIER DENTAL PRODUCTS CO.·1 product·🇺🇸 United States

UNIT, CRYOSURGICAL, ACCESSORIES

FDA registration

SONTEC INSTRUMENTS, INC.·1 product·🇺🇸 United States

CryoClear

FDA registration

CRYOCONCEPTS LP·1 product·🇺🇸 United States

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112618·BARRON CORNEAL PUNCH 7.5MM

VARIANT

FDA UDI

CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1020760·Trial 30x38mm, 8° Lordotic, 15mm

COVERIS

FDA UDI

CAMBER SPINE TECHNOLOGIES, LLC·B030CS1020760·Trial, 12 x 14.5mm, 3° Lordotic, 8mm

Femoral Notch Guide 1

FDA UDI

SIGNATURE ORTHOPAEDICS PTY LTD·09348215056339·

FlexCath steerable sheath

FDA registration

Sterigenics EO Canada, Inc.·1 product·🇨🇦 Canada

JHS / DIFFERENTIAL RATE KINETIC METHOD, CPK OR ISOENZYMES

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

Frozen Format LA Confirm

FDA registration

DSRV, INC.·1 product·🇺🇸 United States

CKMB UDR

FDA registration

SENTINEL CH. SPA·1 product·🇮🇹 Italy

PROWESS PANTHER PROARC, MODEL VERSION 5.0

FDA 510(k)

FDA Class 2 ·Radiology

ATRIUM C-QUR OVT MESH

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

System, Planning, Radiation Therapy Treatment

FDA classification

FDA Class 2 ·System, Planning, Radiation Therapy Treatment