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DJO, LLC

Last updated September 17, 2026

Information

Country: US
Address: 5919 Sea Otter Place, Carlsbad, CA, 92010
Website: djoglobal.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 760-734-3161
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3017264244
DUNS Number: 081840873

Catalogue (2587)

Page 47 of 52

Device	Model / Reference	Registries	Class	Status
Djo Surgical	323-01-103	FDA UDI	Class II	Active
Aircast	30A	FDA UDI	Class II	Unknown
Djo Surgical	801-01-495	FDA UDI	Class I	Active
Djo Surgical	803-61-061	FDA UDI	Class I	Active
Chattanooga	2788-2	FDA UDI	Class II	Active
Aircast	11C	FDA UDI	Class II	Active
Djo Surgical	802-05-002	FDA UDI	Class I	Active
Bell-Horn	110002X	FDA UDI	Class II	Active
Chattanooga	78047	FDA UDI	Class II	Active
Donjoy	11-2015-6	FDA UDI	Class I	Active
Donjoy	11-1640	FDA UDI	Class II	Active
Chattanooga	INT001	FDA UDI	Class II	Active
Djo Surgical	800-01-140	FDA UDI	Class I	Active
Djo Surgical	801-01-538	FDA UDI	Class I	Active
Djo Surgical	804-00-029	FDA UDI	Class I	Active
Djo Surgical	803-05-165	FDA UDI	Class I	Active
Donjoy Performance	DP151KB05-SGR-XL-R	FDA UDI	Class I	Active
Bell-Horn	112103X-LONG	FDA UDI	Class II	Active
Bell-Horn	11248S	FDA UDI	Class II	Active
Djo Surgical	803-05-239	FDA UDI	Class I	Active
Chattanooga	4018	FDA UDI	Class I	Active
Djo Surgical	801-01-660	FDA UDI	Class I	Active
Procare	155-81-87305	FDA UDI	Class I	Active
Aircast	01F241	FDA UDI	Class I	Active
Djo Surgical	803-00-089	FDA UDI	Class I	Active
Djo Surgical	801-01-517	FDA UDI	Class I	Active
Non Franchise	88-578000727030	FDA UDI	Class I	Active
Non Franchise	88-578000372071	FDA UDI	Class I	Active
Chattanooga	2026	FDA UDI	Class I	Active
Donjoy	11-1630-1978	FDA UDI	Class II	Active
Bell-Horn	113402X	FDA UDI	Class II	Unknown
Bell-Horn	11210XL	FDA UDI	Class II	Active
Procare	155-79-87075	FDA UDI	Class I	Active
Donjoy	11-0680-9-00000	FDA UDI	Class II	Active
Compex	CX172EL02-5PK	FDA UDI	Class II	Active
Chattanooga	7550	FDA UDI	Class II	Active
Chattanooga	77615	FDA UDI	Class II	Active
Chattanooga	2795-10	FDA UDI	Class II	Active
Djo Surgical	804-06-013	FDA UDI	Class I	Active
Procare	79-87297-0178	FDA UDI	Class I	Active
Chattanooga	1506-1	FDA UDI	Class II	Active
Chattanooga	6876-4-X	FDA UDI	Class II	Active
Chattanooga	6874-1-X	FDA UDI	Class II	Active
Procare	79-95328-4074	FDA UDI	Class I	Active
Djo Surgical	800-01-178	FDA UDI	Class I	Active
Djo Surgical	804-00-075	FDA UDI	Class I	Active
Chattanooga	5000033	FDA UDI	Class II	Active
Bell-Horn	11310XL	FDA UDI	Class II	Unknown
Djo Surgical	803-04-332	FDA UDI	Class I	Active
Djo Surgical	803-61-106	FDA UDI	Class I	Active

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FDA Recalls (11)

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
Mar 19, 2026	Z-2134-2026	—	open, classified	Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Mar 19, 2026	Z-2135-2026	—	open, classified	Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Mar 19, 2026	Z-2136-2026	—	open, classified	Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Mar 19, 2026	Z-2137-2026	—	open, classified	Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Sep 25, 2025	Z-0722-2026	—	open, classified	The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures capable of causing a second degree burn.
Sep 7, 2021	Z-0009-2022	—	open, classified	Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Sep 7, 2021	Z-0010-2022	—	open, classified	Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Jan 17, 2019	Z-1985-2019	—	open, classified	The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
Jun 25, 2018	Z-2590-2020	—	terminated	The device accessories were not labeled with appropriate latex warning.
Aug 21, 2015	Z-0121-2016	—	terminated	Overheating and burning of the wire insulation inside the applicator.
May 28, 2013	Z-1661-2013	—	terminated	DJO, LLC has recently identified a product safety issue with the battery assembly for the VenaFlow 30B-B and 30 BI-B products. There is a potential for battery leakage which could result in thermal meltdown (fire).