Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Life Spine, Inc. — Predicate Candidate Screening

85 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

91 daysmedian FDA review time
260 days90th percentile
85clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K261430TruLift Expandable SystemLife Spine, Inc.2026-07-28890
K260571SIMPACT Sacroiliac Joint Fixation System GX Navigation InstrLife Spine, Inc.2026-06-021030
K260837VersaLift Expandable SystemLife Spine, Inc.2026-05-12600
K254274ARx® SAI Implant SystemLife Spine, Inc.2026-04-161070
K253748Life Spine ProLift & ProLift Lateral and ProLift Lateral FixLife Spine, Inc.2026-01-23590
K251502TruLift® Lateral Expandable Spacer & Lateral Buttress Plate Life Spine, Inc.2025-07-07530
K250373ProLift Expandable Spacer SystemLife Spine, Inc.2025-04-09580
K243668ProLift Pivot Expandable Spacer SystemLife Spine, Inc.2025-01-23570
K243369Cervical Plating SystemLife Spine, Inc.2024-12-11420
K242826ProLift Wedge Expandable Spacer SystemLife Spine, Inc.2024-10-08200
K241464ARx® SAI Implant SystemLife Spine, Inc.2024-07-29670
K233455ARx MIS Spinal Screw SystemLife Spine, Inc.2023-12-12530
K232611TruLift Micro Expandable Spacer System & TruLift Expandable Life Spine, Inc.2023-11-30940
K231704Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer SystemLife Spine, Inc.2023-10-191290
K223430ProLift Micro Expandable Spacer SystemLife Spine, Inc.2023-05-041710
K221806TruLift Lateral Expandable Spacer System & Lateral Plate SysLife Spine, Inc.2022-12-051660
K222628Life Spine ALIF Buttress Plate SystemLife Spine, Inc.2022-11-16770
K213417Ghost Spacer SystemLife Spine, Inc.2022-09-293440
K220341ARx Modular Spinal SystemLife Spine, Inc.2022-05-02840
K220025ARx® Spinal SystemLife Spine, Inc.2022-03-31850
K212903SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.2021-12-15930
K212520ProLift Micro Expandable Spacer SystemLife Spine, Inc.2021-10-08590
K202836GX Navigation Instrument SystemLife Spine, Inc.2021-08-193280
K210061ProLift Lateral HELO FixatedLife Spine, Inc.2021-04-301090
K210549ARx Spinal SystemLife Spine, Inc.2021-04-22560
K203361ProLift Wedge Expandable Spacer SystemLife Spine, Inc.2021-03-171210
K203163ARx Illiac Spinal Screw SystemLife Spine, Inc.2020-12-17550
K201538Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.2020-09-181010
K201721TruLift Expandable Spacer SystemLife Spine, Inc.2020-09-04730
K201500Life Spine Plateau-A Ti Anterior Lumbar Spacer & Plateau-X TLife Spine, Inc.2020-08-04600
K200896Solstice CCILife Spine, Inc.2020-04-28250
K200070ARx Spinal SystemLife Spine, Inc.2020-04-231010
K200338ProLift Lateral FixatedLife Spine, Inc.2020-04-17660
K193521Steerable Plateau TiLife Spine, Inc.2020-02-06490
K193258ProLift Expandable SystemLife Spine, Inc.2020-01-31660
K191834Stand-Alone ALIF Titanium SystemLife Spine, Inc.2019-12-161600
K190721LongBow TiLife Spine, Inc.2019-11-142390
K191927Hinged Laminoplasty SystemLife Spine, Inc.2019-09-20630
K191575ARx Spinal SystemLife Spine, Inc.2019-08-08550
K190488ProLift Expandable SystemLife Spine, Inc.2019-07-231450
K191005ProLift® Expandable SystemLife Spine, Inc.2019-06-13580
K183430Modular Spinal Fixation SystemLife Spine, Inc.2019-03-13920
K181625Life Spine Resolute™ Threaded Cage SystemLife Spine, Inc.2018-12-111740
K181717Life Spine Laminoplasty SystemLife Spine, Inc.2018-10-121060
K180215DYNA-LINK ELITE Stand-Alone Anterior Lumbar SystemLife Spine, Inc.2018-09-132310
K173883External Fixation SystemLife Spine, Inc.2018-09-072600
K180166Life Spine Lumbar Fixation System (SENTRY)Life Spine, Inc.2018-06-221510
K180749Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.2018-06-15850
K180642Pro-Link® Ti Stand-Alone Cervical Spacer SystemLife Spine, Inc.2018-05-10590
K172105The Plateau-LO Spacer SystemLife Spine, Inc.2018-02-022050

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda