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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 17 of 52

Device	Model / Reference	Registries	Class	Status
Djo Surgical	800-01-054	FDA UDI	Class I	Active
Djo Surgical	803-10-002	FDA UDI	Class I	Active
Chattanooga	101141	FDA UDI	Class II	Active
Djo Surgical	804-03-039	FDA UDI	Class I	Active
Donjoy Performance	DP151KB02-SGR-XL	FDA UDI	Class I	Active
Procare	155-81-97043	FDA UDI	Class I	Active
Chattanooga	5000008	FDA UDI	Class II	Active
Djo Surgical	800-01-033	FDA UDI	Class I	Active
Djo Surgical	804-03-041	FDA UDI	Class I	Active
Djo Surgical	804-02-035	FDA UDI	Class I	Active
Procare	79-80090	FDA UDI	Class I	Active
Djo Surgical	803-04-099	FDA UDI	Class I	Active
Djo Surgical	80101164	FDA UDI	Class I	Active
Djo Surgical	803-21-027	FDA UDI	Class I	Active
Djo Surgical	804-00-040	FDA UDI	Class I	Active
Bell-Horn	200104X	FDA UDI	Class II	Active
Bell-Horn	11864E	FDA UDI	Class II	Unknown
Djo Surgical	931-36-768	FDA UDI	Class II	Active
Chattanooga	59056	FDA UDI	Class II	Active
Chattanooga	18080-R	FDA UDI	Class I	Active
Chattanooga	42192	FDA UDI	Class II	Active
Djo Surgical	803-06-022	FDA UDI	Class I	Active
Aircast	2130	FDA UDI	Class II	Active
Chattanooga	8250	FDA UDI	Class II	Active
Donjoy Performance	DP151KB06-BLK-M	FDA UDI	Class I	Active
Aircast	13B01	FDA UDI	Class II	Active
Procare	79-87283-4074	FDA UDI	Class I	Active
Chattanooga	8200	FDA UDI	Class I	Active
Djo Surgical	803-05-050	FDA UDI	Class I	Active
Aircast	500R-2	FDA UDI	Class II	Active
Aircast	3004	FDA UDI	Class II	Unknown
Djo Surgical	800-01-061	FDA UDI	Class I	Active
Djo Surgical	233-08-106	FDA UDI	Class II	Active
Donjoy Performance	DP171SR01-BLK	FDA UDI	Class I	Active
Chattanooga	5000060	FDA UDI	Class II	Active
Chattanooga	42180	FDA UDI	Class II	Active
Djo Surgical	801-01-405	FDA UDI	Class I	Active
Donjoy	11-1631-0429	FDA UDI	Class II	Active
Bell-Horn	11810L	FDA UDI	Class II	Active
Djo Surgical	202-09-106	FDA UDI	Class II	Active
Bell-Horn	11814L	FDA UDI	Class I	Active
Donjoy Performance	DP157ES01-BLK-M	FDA UDI	Class I	Active
Bell-Horn	11330S	FDA UDI	Class II	Unknown
Bell-Horn	113002X	FDA UDI	Class II	Active
Donjoy Performance	DP151AB05-BLK-L-R	FDA UDI	Class I	Active
Procare	79-90175	FDA UDI	Class I	Active
Chattanooga	27314	FDA UDI	Class II	Active
Bell-Horn	20020M	FDA UDI	Class II	Active
Djo Surgical	803-84-538	FDA UDI	Class I	Active
Djo Surgical	801-01-503	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).