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Micromedics, Inc.

United States·US-MF-000018365

Last updated September 17, 2026

Information

Country: United States
Address: 1270, Eagan Industrial Road , St. Paul, United States
Website: nordsonmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 651.236.7869
PRRC Contact: Nicole Freeberg
EUDAMED SRN: US-MF-000018365
FDA FEI Number: 2183425
DUNS Number: 066839630

Catalogue (231)

Page 2 of 5

Device	Model / Reference	Registries	Class	Status
Mitek Sports Medicine	278013	FDA UDI	Class I	Active
Duplospray	0600029	FDA UDI	Class II	Unknown
Fibrijet	SA-3655	FDA UDI	Class II	Active
Nordson Medical	SA-3663	FDA UDI	Class II	Active
Duplospray	0601130	FDA UDI	Class II	Active
Actamax	AX-310	FDA UDI	Class II	Active
OsteoPrecision	ABS-10054-10	FDA UDI	Class II	Active
Gasless Tip	601151	FDA UDI	Class I	Active
Mitek Sports Medicine	278015	FDA UDI	Class I	Active
Fibrijet	SA-3445	FDA UDI	Class I	Active
Celling Biosciences Versatile Delivery Kit	0861-0003	FDA UDI	Class I	Active
Duplotip	SA374003004444	FDA UDI	Class II	Active
OsteoPrecision	GD-1015-150-CC	FDA UDI	Class II	Active
FibriJet	SA-3677	FDA UDI	Class I	Active
Biocomposites	990-001	FDA UDI	Class II	Active
OsteoExpress	GDNS-5215	FDA UDI	Class II	Active
FibriJet	800-0225	FDA UDI	Class I	Active
Nordson Medical	5125000	FDA UDI	Class II	Active
Fibrijet	SA-3650	FDA UDI	Class II	Unknown
OsteoPrecision	ABS-10054-15	FDA UDI	Class II	Active
Duplotip	0601138	FDA UDI	Class II	Active
Mitek Sports Medicine	278012	FDA UDI	Class I	Active
Mitek Sports Medicine	278011	FDA UDI	Class I	Active
Duplospray	0600033	FDA UDI	Class II	Active
Discseel	DISC-3CC	FDA UDI	Class I	Active
Celling Biosciences	CB-5515	FDA UDI	Class II	Active
Medtronic Resilant	779101	FDA UDI	Class II	Unknown
Biomet Biologics	800-0250	EUDAMED	Class IIa	Active
Biomet Biologics	800-0202	EUDAMED	Class IIa	Active
LifeSpine	LS-1015-150Z	EUDAMED	Class IIa	Active
Arthrex BioXpress	ABS-10053-15-45	EUDAMED	Class IIa	Active
Arthrex Applicator	ABS-10051	EUDAMED	Class IIa	Active
OsteoPrecision	GD-1115-150	EUDAMED	Class IIa	Active
Biomet Biologics	800-0201	EUDAMED	Class IIa	Active
Arthrex BioXpress	ABS-10053-10-45	EUDAMED	Class IIa	Active
Biomet Rigid Endoscopic Tip	800-0208	EUDAMED	Class IIa	Active
Biomet Biologics	800-0202	EUDAMEDFDA UDI	Class IIa	Active
OsteoPrecision	GD-1215-150	EUDAMEDFDA UDI	Class IIa	Active
Arthrex BioXpress	ABS-10053-15	EUDAMEDFDA UDI	Class IIa	Active
Arthrex Applicator	ABS-10050	EUDAMED	Class IIa	Active
Arthrex BioXpres	ABS-10053-15	EUDAMED	Class IIa	Active
Baxter Gasless Replacement Tips	601160	EUDAMED	Class IIa	Active
LifeSpine	LS-1015-150Z	EUDAMEDFDA UDI	Class IIa	Active
Baxter Gasless Tip Applicator	601159	EUDAMED	Class IIa	Active
Biomet Rigid Endoscopic Tip	800-0208	EUDAMED	Class IIa	Active
Arthrex BioXpress	ABS-10053-10	EUDAMEDFDA UDI	Class IIa	Active
Biomet Biologics	800-0201	EUDAMEDFDA UDI	Class IIa	Active
OsteoXpress	GD-5515	EUDAMED	Class IIa	Active
OsteoPrecision	GD-1215-150	EUDAMED	Class IIa	Active
Micromedics Surgical Instruments	K842212	FDA 510(k)	N/A	Active

Related Companies

Authorised Representatives

MDSS GmbH DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (5)

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
Oct 20, 2016	Z-1817-2017	—	terminated	The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may affect sterility assurance.
Mar 15, 2010	Z-0347-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.
Mar 15, 2010	Z-0348-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.
Mar 15, 2010	Z-0346-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches potentially resulting in a non-sterile product which may cause transmission of disease or infection.
Mar 15, 2010	Z-0345-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.