Globus Medical, Inc.
Globus Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2026, with 29 FDA device recalls on record.
Clearances by Globus Medical, Inc. — page 2
101–175 of 175- K133350 — REVERE STABILIZATION SYSTEM
- K133567 — UNIFY(R) DYNAMIC ANTERIOR CERVICAL PLATE SYSTEM
- K132559 — MONUMENT SPACERS
- K130977 — SIGNIFY BIOACTIVE
- K132191 — SP-FIX SPINOUS PROCESS FIXATION PLATE
- K130392 — KINEX BIOACTIVE
- K131449 — COALITION SPACER
- K130478 — SUSTAIN AND SUSTAIN RADIOLUCENT SPACERS
- K123913 — LATIS SPACER
- K124058 — CREO STABILIZATION SYSTEM
- K123783 — ELLIPSE OCCIPITO-CERICO-THORACIC SPINAL SYSTEM AND CAPITOL IMPLANTS
- K123231 — CALIBER SPACERS
- K122097 — PATRIOT SPACERS
- K121732 — CANOPY LAMINOPLASTY FIXATION SYSTEM
- K122226 — REVERE STABILIZATION SYSTEM
- K121922 — BEACON STABILIZATION SYSTEM
- K121107 — FORTIFY INTEGRATED CORPECTOMY SPACERS, (FORTIFY I AND FORTIFY I-R)
- K121049 — UNIFY DYNAMIC ANTERIOR CERVICAL PLATE SYSTEM
- K113395 — REVERE 4.5 STABILIZATION SYSTEM
- K120092 — PLYMOUTH THORACOLUMBAR PLATE SYSTEM
- K120101 — INDEPENDENCE SPACER
- K113447 — RISE SPACER
- K112028 — SI-LOK SACROILIAC JOINT FIXATION SYSTEM
- K112756 — FORTIFY(TM) AND FORTIFY(TM)-R CORPECTOMY SPACERS
- K111449 — REVOLVE ADDITIONAL IMPLANTS
- K111479 — REVERE CROSSTOP
- K110280 — REVLOK FENESTRATED SCREW SYSTEM
- K103382 — INTERCONTINENTAL PLATE-SPACER
- K110963 — ELLIPSE OCCIPITO-CERVICO-THORACIC SPINAL SYSTEM
- K103072 — REVERE SACRAL PLATES
- K102195 — SP-FIX SPINOUS PROCESS FIXATION PLATE
- K102293 — CALIBER SPACER
- K102392 — MICROFUSE PUTTY AND MICROFUSE ST MIS
- K102313 — PATRIOT TRANSCONTINENTAL M SPACERS
- K100788 — COCR RODS
- K093294 — REVERE STABILIZATION SYSTEM
- K093242 — PATRIOT TRANSCONTINENTAL LLIF SPACER
- K092146 — XTEND ANTERIOR CERVICAL PLATE SYSTEM
- K092610 — MODIFICATION TO BEACON STABILIZATION SYSTEM
- K091782 — REVERE 6.35 STABILIZATION SYSTEM
- K092108 — TRUSS THORACOLUMBAR PLATE SYSTEM
- K090952 — ZYFUSE FACET FIXATION SYSTEM
- K090565 — ELLIPSE OCCIPITO-CERICO-THORACIC SPINAL SYSTEM
- K083389 — COALITION SPACER
- K073439 — TRANSITION STABILIZATION SYSTEM
- K083442 — CORRIDOR FIXATION SYSTEM
- K083416 — REVOLVE STABILIZATION SYSTEM
- K083232 — MODIFICATION TO:MICROFUSE BONE VOID FILLER
- K081906 — PROTEX CT CERVICOTHORACIC SPINAL SYSTEM
- K082252 — INDEPENDENCE SPACER
- K082442 — MODIFICATION TO MICROFUSE BONE VOID FILLER
- K080664 — RELIEVE LAMINOPLASTY FIXATION SYSTEM
- K081391 — VIP ANTERIOR CERVICAL PLATE SYSTEM
- K081195 — REVERE UNIPLANAR SCREWS
- K072970 — PATRIOT SPACERS
- K072991 — PATRIOT SPACERS: COLONIAL ACDF
- K073517 — H-LINK INTEGRATED ROD
- K071187 — MICROFUSE BONE VOID FILLER
- K073172 — BEACON STABILIZATION SYSTEM
- K072465 — NIKO CORPECTOMY SPACER
- K070775 — MODIFICATION TO: PROVIDENCE ANTERIOR CERVICAL PLATE SYSTEM
- K062836 — CITADEL ANTERIOR LUMBAR PLATE SYSTEM
- K062407 — GATEWAY THORACOLUMBAR PLATE SYSTEM
- K061202 — REVERE STABILIZATION SYSTEM
- K061380 — RETAIN RADIOLUCENT SPACER
- K060665 — XPAND RADIOLUCENT CORPECTOMY SPACER
- K052069 — PROTEX STABILIZATION SYSTEM WITH ADDITIONAL COMPONENTES
- K050391 — PROTEX CT CERVICOTHORACIC SPINAL SYSTEM
- K050850 — XPAND CORPECTOMY SPACER
- K042168 — CONCORD Radiopaque Bone Cement
- K042953 — MODIFICATION TO PROTEX STABILIZATION SYSTEM
- K040721 — ASSURE ANTERIOR CERVICAL PLATE SYSTEM
- K040442 — PROTEX STABILIZATION SYSTEM
- K040284 — SUSTAIN RADIOLUCENT SPACER
- K031302 — SUSTAIN SPACER
Data sourced from openFDA. This site is unofficial and independent of the FDA.