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Aptos, LLC

Active in EUDAMED

Georgiafrom SRN EUDAMED SRN GE-MF-000020012

Aptos, LLC is a medical device manufacturer based in Georgia, with 15 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (EU Class III, IIb and IIa; FDA Class II) as of 12 Nov 2026.

Devices
15
Registrations
EUDAMED

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • EUDAMED 12
  • FDA GUDID 2
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • EU Class III 6
  • EU Class IIb 5
  • FDA Class II 3
  • EU Class IIa 1
Top EMDN categories
Sites and related companies
Identifiers
  • EUDAMED SRN GE-MF-000020012
  • DUNS 360531712

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
Authorised rep.
MDSS GmbHDE

What Aptos, LLC makes

Aptos, LLC manufactures monofilament sutures made from polyolefin and fluoropolymer materials, including polypropylene-based surgical sutures. These products are designed for use in various surgical procedures requiring durable, tissue-friendly thread.

The company’s devices are regulated under EU Medical Device Regulations (Class II, IIa, IIb, and III) and U.S. FDA pathways, including 510(k) clearances and UDI listings. Their products are recorded in the EUDAMED database and the FDA’s device registries, with operations based in Georgia, USA.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue15

Newest first, rows 1-15 of 15

Search and filter all 15 devices
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  • Aptos Ref EVSHA004

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Aptos Needle 2G Soft Large

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Aptos Thread 2G

    Active Regimes: 510(k) Registry: GUDID Class:II
  • APTOS Threads – Polypropylene Surgical Sutures Ref K192953

    Active Regimes: CE MDD 510(k) Registry: 510(k) Class:II
  • Aptos Ref NEHA007

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Aptos Ref AN4.0030

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Aptos Ref AW3.0034

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Aptos Ref ASS024

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Aptos Ref NV7021

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Aptos Ref AN2GSL026

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Aptos Ref AN2.0029

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Aptos Ref NE006

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Aptos Ref IEMHA009

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Aptos Ref DRN031

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Aptos Ref LLN2GSL016

    Active Regimes: CE MDD Registry: EUDAMED Class:III

Rows 1-15 of 15

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
GE-MF-000020012
DUNS number
360531712
EU VAT number
202353602
EUDAMED status
Active
EUDAMED registered name
Aptos LLC
Registered address
15, Givi Amilakhvari Street, 0109, Tbilisi, Georgia
Phone
+995322910372
PRRC contact
Tamara Beshidze(public in EUDAMED)

Frequently asked questions

How many devices does Aptos, LLC have in the registry?

The registry currently lists 15 devices for Aptos, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aptos, LLC's devices?

Among its 15 most recently registered devices, Aptos, LLC has devices listed in EUDAMED (12 devices), FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Aptos, LLC's devices fall under?

Among its 15 most recently registered devices, the classes recorded for Aptos, LLC's devices are Class IIa, Class IIb, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Aptos, LLC in the registry?

The most recently registered devices listed for Aptos, LLC include APTOS, Aptos Needle 2G Soft Large, Aptos Thread 2G and APTOS Threads – Polypropylene Surgical Sutures.

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