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Intrinsic Therapeutics

Last updated September 17, 2026

Information

Country: US
Address: 30 Commerce Way, Woburn, MA, 01801
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3006232063
DUNS Number: —

Catalogue (29)

Device	Model / Reference	Registries	Class	Status
Nerve Root Suction-Retractor	400904	FDA UDI	Class I	Active
Barricaid® ACD (Annular Closure Device)	10mm width	FDA UDI	Class III	Active
Barricaid® ACD - Reusable Instruments Kit	4001007	FDA UDI	N/A	Active
Defect Measurement Tool (4/5mm)	400209	FDA UDI	N/A	Unknown
Defect Measurement Tool (6/7mm)	400210	FDA UDI	N/A	Unknown
Barricaid ACD Sizing Trial (10mm)	400877	FDA UDI	N/A	Unknown
Defect Measurement Tool (12/13mm)	400213	FDA UDI	N/A	Active
Barricaid ACD Retraction Wedge	400846	FDA UDI	N/A	Unknown
Defect Measurement Tool (12/13mm)	400213	FDA UDI	N/A	Unknown
Barricaid® ACD Alignment Trial (8mm)	400879	FDA UDI	N/A	Active
Defect Measurement Tool (4/5mm)	400209	FDA UDI	N/A	Active
Barricaid® ACD Impactor	400906-A	FDA UDI	Class I	Active
Barricaid® ACD - Reusable Instruments Kit (Tray Only)	400885	FDA UDI	N/A	Active
Barricaid® ACD Alignment Trial (10mm)	400877	FDA UDI	N/A	Active
Defect Measurement Tool (10/11mm)	400212	FDA UDI	N/A	Unknown
Barricaid ACD Sizing Trial (8mm)	400879	FDA UDI	N/A	Unknown
Barricaid ACD Impactor	400906	FDA UDI	N/A	Unknown
Defect Measurement Tool (6/7mm)	400210	FDA UDI	N/A	Active
Barricaid® ACD Retraction Wedge	400846	FDA UDI	N/A	Active
Barricaid® ACD (Annular Closure Device)	8mm width	FDA UDI	Class III	Active
Surgical Hammer	400896	FDA UDI	N/A	Unknown
Defect Measurement Tool (10/11mm)	400212	FDA UDI	N/A	Active
Barricaid® ACD - Reusable Instruments Kit	4001004	FDA UDI	N/A	Active
Defect Measurement Tool (8/9mm)	400211	FDA UDI	N/A	Active
Barricaid ACD Extractor	400763/400766	FDA UDI	N/A	Unknown
Surgical Mallet (Slotted)	400929	FDA UDI	N/A	Active
Barricaid® ACD Removal Tool	400921-A	FDA UDI	Class I	Active
Defect Measurement Tool (8/9mm)	400211	FDA UDI	N/A	Unknown
Barricaid Anular Closure Device (ACD)	P160050	FDA PMA	Class III	Active

Related Companies

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FDA Recalls (2)

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

Date	Recall No.	Class	Status	Reason
Jul 25, 2024	Z-2688-2024	—	open, classified	At least two units have been found to be missing a weld.
Jul 24, 2020	Z-2798-2020	—	terminated	The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.