Digital Lab Analog Screw DDLAWS

by Dentis Co., Ltd

Digital Lab Analog Screw DDLAWS is a Class I device made by Dentis Co., Ltd, listed in FDA GUDID since 20 Aug 2024 (UDI-DI 08800266941619), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08800266941619 UDI-DI	Date20 Aug 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 08800266941619

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Digital Lab Analog Screw
Generic name: Dental implant analog
Model / reference: DDLAWS

Primary DI / UDI-DI: 08800266941619
FDA product code: NDP
GMDN term: Dental implant analog

Device class: Class I
Regulation number: 872.3980
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Single use
Prescription use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (9, all answered No)