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Integrity Implants Inc.

United States·US-MF-000009805

Last updated May 24, 2026

Information

Country
United States
Address
354, Hiatt Drive, Palm Beach Gardens, United States
LinkedIn
—
Facebook
—
Phone
+1 561 529 3861
PRRC Contact
Natalia Giaquinta
EUDAMED SRN
US-MF-000009805
FDA FEI Number
—
DUNS Number
080300717

Catalogue (1530)

Page 3 of 31
DeviceModel / ReferenceRegistriesClassStatus
LineSider LS-N6SG6535
FDA UDI
Class IIActive
LineSider LS-SC7A6535
FDA UDI
Class IIActive
LineSider LS-SC7L5050
FDA UDI
Class IIActive
LineSider LS-SC7R8580
FDA UDI
Class IIActive
LineSider LS-RD55A050
FDA UDI
Class IIActive
FlareHawk ASY-00048
FDA UDI
Class IIActive
LineSider LS-N6RA7550
FDA UDI
Class IIActive
LineSider LS-SC7E7530
FDA UDI
Class IIActive
LineSider LS-N6RA5545
FDA UDI
Class IIActive
LineSider LS-N6SE4535
FDA UDI
Class IIActive
LineSider LS-N6RA6530
FDA UDI
Class IIActive
LineSider LS-RD55H500
FDA UDI
Class IIActive
LineSider LS-N6RA7545
FDA UDI
Class IIActive
LineSider LS-N6MG7550
FDA UDI
Class IIActive
LineSider LS-N6RA5060
FDA UDI
Class IIActive
FlareHawk CMP-00829
FDA UDI
Class IIActive
Toro-L CMP-02581
FDA UDI
Class IIActive
LineSider LS-SC7G8555
FDA UDI
Class IIActive
LineSider LS-N6SG8555
FDA UDI
Class IIActive
LineSider LS-N6RG7540
FDA UDI
Class IIActive
LineSider LS-N6SA9550
FDA UDI
Class IIActive
LineSider LS-SC7G4520
FDA UDI
Class IIActive
LineSider LS-N6CR1590
FDA UDI
Class IIActive
LineSider LS-SC7L7560
FDA UDI
Class IIActive
LineSider LS-N6SA5060
FDA UDI
Class IIActive
FlareHawk II-1-0453
FDA UDI
Class IIActive
FlareHawk FHTAS30623O
FDA UDI
Class IIActive
LineSider LS-SC7A8535
FDA UDI
Class IIActive
LineSider LS-N6MG4535
FDA UDI
Class IIActive
FlareHawk FHTGCT0029TTS
FDA UDI
Class IIActive
LineSider LS-RD55D060
FDA UDI
Class IIActive
LineSider LS-SC7G5055
FDA UDI
Class IIActive
LineSider LS-N6RG8560
FDA UDI
Class IIActive
LineSider LS-N6SA1540
FDA UDI
Class IIActive
Accelus Navigated Reusable Instruments ASY-00729
FDA UDI
Class IIActive
LineSider LS-N6RG5060
FDA UDI
Class IIActive
LineSider LS-N6SG5055
FDA UDI
Class IIActive
LineSider LS-N6CR7590
FDA UDI
Class IIActive
Toro-L TL10-002460
FDA UDI
Class IIActive
LineSider LS-N6SE5555
FDA UDI
Class IIActive
LineSider LS-N6SE5020
FDA UDI
Class IIActive
LineSider LS-N6RA9545
FDA UDI
Class IIActive
LineSider LS-N6MG1560
FDA UDI
Class IIActive
LineSider LS-SC7L6530
FDA UDI
Class IIActive
LineSider LS-SC7R9570
FDA UDI
Class IIActive
LineSider LS-N6SE7555
FDA UDI
Class IIActive
LineSider LS-N6ME5020
FDA UDI
Class IIActive
LineSider LS-N6SG1560
FDA UDI
Class IIActive
LineSider LS-SC7A4530
FDA UDI
Class IIActive
LineSider LS-N6ME6550
FDA UDI
Class IIActive

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (6)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Dec 20, 2024Z-1008-2025—open, classified

Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).

Aug 3, 2022Z-0421-2023—terminated

Potential for intraoperative screw head separation at weld location.

Jan 27, 2022Z-0418-2023—terminated

Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.

Jan 27, 2022Z-0420-2023—terminated

Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.

Jan 27, 2022Z-0419-2023—terminated

Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.

Feb 27, 2018Z-0405-2019—terminated

Recently Integrity Implants uncovered a discrepancy in the cleaning parameters in several of their labeling material. The firm is initiating the field correction to ensure that updated information is provided to all accounts.