Ctl Medical Corporation
Ctl Medical Corporation holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2024, with 6 FDA device recalls on record.
Top product codes for Ctl Medical Corporation
FDA recalls by Ctl Medical Corporation
- Z-2504-2020 — CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H8mm, Part #018.1908.
- Z-2501-2020 — CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H7mm, Part #018.1307.
- Z-2502-2020 — CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907.
- Z-2503-2020 — CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H8mm, Part #018.1308.
- Z-1030-2019 — CTL Medical Hex Driver, 1/4" Square QC, 4.0 Ratcheting Ref 015.7050
- Z-1031-2019 — CTL Medical Hex Driver MIS, 1/4" Square QC, 4.0 Ratcheting Ref 019.7050
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ctl Medical Corporation
- K233947 — KLIMT Expandable Lumbar Interbody Fusion (LIF) Cage System
- K231715 — MONDRIAN Anterior Lumbar Plate System
- K231359 — RODIN Expandable Lumbar Cage System
- K220513 — NITRO Interbody Fusion Cage System Family
- K220334 — MONET Anterior Cervical Plate System
- K211785 — CASSATT SIJ Fixation System
- K213641 — MONDRIAN ALIF Cage with Supplementary Fixation Plate
- K213491 — Universal Pilot Guidance Instrument System
- K192863 — MONDRIAN Lumbar Interbody Fusion Cage System
- K182151 — MONET Anterior Cervical Interbody Fusion Cage System with Supplementary Fixation Plate
- K172788 — MONET Anterior Cervical Interbody Fusion Cage System
- K173185 — SEURAT Universal Pedicle Screw System
- K172212 — MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK
- K162682 — MATISSE Anterior Cervical Interbody Fusion Cage System
Data sourced from openFDA. This site is unofficial and independent of the FDA.