DemeLON NL13x1650

by DemeTECH Corp

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10652927269625 UDI-DI	Date15 Jul 2019Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: DemeLON
Generic Name: Nylon suture, non-bioabsorbable, monofilament
Model / Reference: NL13x1650

Primary DI / UDI-DI: 10652927269625
510(k) Number: K023028
FDA Product Code: GAR
GMDN Term: Nylon suture, non-bioabsorbable, monofilament

Device Class: Class II
Regulation Number: 878.5020
GUDID distribution status: In Commercial Distribution

Other devices from DemeTECH Corp

DemeLON

Class IIb
DemeSILK

Class IIb
DemeSORB

Class III
DemeCAPRONE

Class III
DemeSTEEL

Class IIb
DemeLENE

Class IIb

See all devices from DemeTECH Corp →

Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (8)

Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No