Clozex Medical, Inc.

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union: EUDAMED actor, 1 certificate
United States: FDA FEI

Catalogue18

Newest first, rows 1-18 of 18

Search and filter all 18 devices

Clozex Wound Closure CL10100L

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1020S

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1015S

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1025S

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1080L

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1060L

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1050L

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1040L

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure LK0150

None Registry: GUDID Class:I
Clozex Wound Closure CL1040S

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure CL1030S

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure LA0360

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure LA3110

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure LK0140

None Registry: GUDID Class:I
Clozex Wound Closure LK0265

None Registry: GUDID Class:I
Clozex Wound Closure LC0240

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure LC0225

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Clozex Wound Closure LA0390

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I

Rows 1-18 of 18

Company details

EUDAMED SRN: US-MF-000029460
FDA FEI number: 3006891462
DUNS number: 138266072
EUDAMED status: Active
EUDAMED registered name: Clozex Medical, Inc.
EUDAMED abbreviated name: CMI
Registered address: 124, Grove Street, 02038, Franklin, United States
Website: www.clozex.com
Facebook: facebook.com/clozexmedical
Email: [email protected]
Phone: +1 781 237 1673
PRRC contact: Nicohl Asher(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 28 May 2031

ENTE CERTIFICAZIONE MACCHINE SRL 1282 1 certificate

ECM26MDR005 Active

Quality management system EU MDR

Issued
29 May 2026

Expires
28 May 2031

Certifiers

ENTE CERTIFICAZIONE MACCHINE SRL 1282

From the company website

Read 18 Oct 2026

Clozex Closures are offered in a full range of sizes for incisions across Surgical Specialties, and treatment of lacerations in the Emergency Response and Urgent Care settings. They range in sizes from 15mm – 100mm and are available in boxes of individual sizes, assorted sizes, and procedure specific kits.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Clozex Medical, Inc. have in the registry?

The registry currently lists 18 devices for Clozex Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clozex Medical, Inc.'s devices?

Among its 18 most recently registered devices, Clozex Medical, Inc. has devices listed in EUDAMED (15 devices) and FDA GUDID (18 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Clozex Medical, Inc.'s devices fall under?

Among its 18 most recently registered devices, the classes recorded for Clozex Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Clozex Medical, Inc.?

EUDAMED lists 1 certificate for Clozex Medical, Inc. (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 29 May 2026.

What are the newest devices from Clozex Medical, Inc. in the registry?

The most recently registered devices listed for Clozex Medical, Inc. include Clozex Wound Closure CL10100L, Clozex Wound Closure CL1020S, Clozex Wound Closure CL1015S and Clozex Wound Closure CL1025S.

Generated automatically from registry data and not verified by a human reviewer.