BEUDAMED
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    FORCE FIBER GREEN ULTRA HIGH MOLECULAR WEIGHT POLYETHYLENE NON ABSORBABLE SUTURES MODEL:X-5000FFK, X-5001FFK, X-5002FFK

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

    Trial Tibial Augment

    FDA UDI
    ADLER ORTHO SPA·08056269044134·TRIAL PANTHEON TIBIAL AUGMENT LM/RL SIZE 6 H5

    GIGLI SAW BLADE HANDLE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896081529·GIGLI SAW BLADE HANDLE LOOP STYLE

    KITZMILLER COOLEY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921005060·KITZMILLER COOLEY CLAMP ANGLED RIGHT

    KITZMILLER COOLEY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896002562·KITZMILLER COOLEY CLAMP ANGLED RIGHT

    PIEZOWAVE2

    FDA UDI
    Richard Wolf GmbH·04055207063989·PIEZOWAVE 2 CONTROL UNIT for all standard indi...

    Precisor Broncho

    FDA UDI
    Conmed Corporation·30653405052122·Precisor® Broncho Biopsy Oval Cup Forceps 1.8 m...

    Indus®

    FDA UDI
    SPINEFRONTIER, INC.·00190361001225·Inset 1 Level ACP, 6mm

    Admiral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981277109·Temporary Fixation Pin

    S-Core™

    FDA UDI
    SUBCHONDRAL SOLUTIONS, INC.·00850017962620·Sizer, 5mm/6 mm

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471155660·V Nat D 016 Lo

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756000512·CERVICAL COLLAR

    ADMIRAL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code KWQ·July 21, 2023

    ADMIRAL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code KWQ·July 21, 2023

    ADMIRAL

    FDA Adverse Event
    Malfunction ·SEASPINE ORTHOPEDICS CORPORATION·Product code LXH·January 13, 2026

    BIO-FASTAK SUTURE ANCHOR, MODEL AR-1324B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HS FIBER (POLYBLEND), RIVER BOND, RIVERSILK (SILK), RIVERPRO (POLYPROPYLENE), RIVERLON (NYLON) MODEL VERIES BY SIZE/NEED

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

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00840326425220·NiTi SE Archwire, NAT .016 Lower Dimple 10EA

    INFANT DUAL-HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·September 17, 2010

    BLUE LINE TRACHEOSTOMY TUBE

    FDA Adverse Event
    Injury ·SMITHS HEALTHCARE MFG S.A. DE C.V.·Product code JOH·September 25, 2006