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Centurion Medical Products

Last updated May 23, 2026

What Centurion Medical Products makes

Centurion Medical Products manufactures single-use surgical procedure kits, including general surgical kits (both medicated and non-medicated), central venous catheterization kits, circumcision kits, peripheral intravenous catheterization support kits, ENT surgical kits, birthing/delivery kits, and procedural medication labeling sets.

The company's portfolio consists of Class I and Class II medical devices, which are listed in the FDA Unique Device Identifier (UDI) registry. Centurion Medical Products is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Centurion Medical Products manufacture?

Centurion Medical Products manufactures single-use surgical procedure kits including general surgical kits (medicated and non-medicated), central venous catheterization kits, circumcision kits, peripheral intravenous catheterization support kits, ENT surgical kits, birthing/delivery kits, and procedural medication labeling sets.

Where is Centurion Medical Products based?

Centurion Medical Products is based in the United States, as indicated in the device registry information.

Which regulatory registries list Centurion Medical Products' devices?

Centurion Medical Products' devices are listed in the FDA Unique Device Identifier (UDI) registry, which tracks medical devices marketed in the United States.

How are Centurion Medical Products' devices classified?

Centurion Medical Products manufactures Class I and Class II medical devices, with Class I being lower risk and Class II requiring more regulatory controls than Class I devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (11015)

Page 3 of 221

Device	Model / Reference	Registries	Class	Status
Centurion	MNS11960	FDA UDI	Class I	Active
Centurion	IVS3310	FDA UDI	Class II	Active
Centurion	CIT4405	FDA UDI	Class II	Active
Centurion	O200ST	FDA UDI	Class II	Active
Centurion	SUT19330	FDA UDI	Class I	Active
Centurion	ECVC1235	FDA UDI	Class II	Active
Centurion	CVI2525	FDA UDI	Class II	Active
Centurion	MNS3680	FDA UDI	Class I	Active
Centurion	CVI2105	FDA UDI	Class I	Active
Centurion	SUT15935	FDA UDI	Class I	Active
Centurion	STL3633	FDA UDI	Class I	Active
Centurion	66440	FDA UDI	Class I	Active
Centurion	DT7550	FDA UDI	Class I	Active
Centurion	DM775B	FDA UDI	Class I	Active
Centurion	DYNJ0182378B	FDA UDI	Class II	Active
Medline Industries, Inc.	ECVC6665	FDA UDI	Class II	Active
Centurion	STL2348	FDA UDI	Class I	Active
Centurion	SUT14915	FDA UDI	Class I	Active
Centurion	SUT17850	FDA UDI	Class I	Active
Centurion	DT13695	FDA UDI	Class I	Active
Centurion	MNS10715	FDA UDI	Class I	Active
Centurion	MNS13115	FDA UDI	Class I	Active
Centurion	BT150	FDA UDI	Class I	Active
Centurion	A2716HKICNL	FDA UDI	Class II	Active
Centurion	CIT5735	FDA UDI	Class II	Active
Centurion	CIT5870A	FDA UDI	Class II	Active
Medline Industries, Inc.	ECVC5165	FDA UDI	Class II	Active
Centurion	CIT5585	FDA UDI	Class II	Active
Centurion	MNS7755A	FDA UDI	Class I	Active
Centurion	ID1180	FDA UDI	Class I	Active
Centurion	ID1525	FDA UDI	Class I	Active
Medline Industries, Inc.	ECVC6940	FDA UDI	Class II	Active
Centurion	BT195	FDA UDI	Class II	Active
Centurion	ECVC5350	FDA UDI	Class II	Active
Centurion	SUT19345	FDA UDI	Class I	Active
Centurion	MNS8025	FDA UDI	Class I	Active
Centurion	CHT790	FDA UDI	Class I	Active
Centurion	STL3778	FDA UDI	Class I	Active
Centurion	STL2065	FDA UDI	Class I	Active
Centurion	DT14240	FDA UDI	Class I	Active
Centurion	66150	FDA UDI	Class I	Active
Centurion	IV7145	FDA UDI	Class II	Active
Centurion	DT20655	FDA UDI	Class I	Active
Centurion	CVI4600	FDA UDI	Class I	Active
Centurion	IV8635	FDA UDI	Class II	Active
Centurion	SV577UDT-6	FDA UDI	Class I	Active
Centurion	SUT15535A	FDA UDI	Class I	Active
Centurion	IV7450	FDA UDI	Class II	Active
Centurion	ID1490	FDA UDI	Class I	Active
Centurion	CHT500	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (100)

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

Centurion Medical Products has 286 recall records initiated between September 22, 2009, and December 11, 2019, all with a status of terminated. The reasons for recall include issues such as compromised sterile packaging, potential for package integrity problems, recalls of components from suppliers due to various concerns like particulate matter, incomplete documentation, and contamination risks. Some recalls were initiated as sub-recalls for products contained in kits that were being recalled by their original manufacturers.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Dec 11, 2019	Z-1075-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1059-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1042-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1082-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1063-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1087-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1068-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1081-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1064-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1083-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1049-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1058-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1047-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1084-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1091-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1053-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1079-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1089-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1052-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1095-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1055-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1050-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1045-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1070-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1094-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1066-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1061-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1065-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1086-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1062-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1051-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1085-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1057-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1060-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1067-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1073-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1044-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1092-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1054-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1056-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1077-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1043-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1088-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1080-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1074-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1076-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1078-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1071-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1069-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1048-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1072-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1090-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1046-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1093-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Oct 24, 2019	Z-0344-2020	—	terminated	Sterile packaging incomplete seals may compromise sterility of the product
Aug 28, 2019	Z-0120-2020	—	terminated	A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
Aug 28, 2019	Z-0121-2020	—	terminated	A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
Jul 15, 2019	Z-0254-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 15, 2019	Z-0255-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 15, 2019	Z-0256-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 15, 2019	Z-0253-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 1, 2019	Z-2165-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2166-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2164-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2171-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2161-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2170-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2168-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2167-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2162-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2172-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2163-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2173-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2169-2019	—	terminated	Potential for sterile packaging to be compromised
Jun 24, 2019	Z-0407-2020	—	terminated	Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer
Jun 24, 2019	Z-0408-2020	—	terminated	Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.
Jun 24, 2019	Z-0409-2020	—	terminated	Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.
Jun 7, 2019	Z-1956-2019	—	terminated	Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.
Jun 1, 2019	Z-2545-2020	—	terminated	False elevation of carboxyhemoglobin (COHb) results in blood samples collected using BD Vacutainer Plastic Lithium Heparin tubes with the IL GEM 4000 instrument.
Apr 24, 2019	Z-0080-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0102-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0103-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0084-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0094-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0081-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0086-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0077-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0085-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0090-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0083-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0075-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0092-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0087-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0105-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0098-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0093-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0106-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0078-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0076-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0096-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.