Core Dynamics CD1935

by Conmed Corporation

Core Dynamics CD1935 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K950457 on 5 May 1995 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20653405055393), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

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	Number20653405055393 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK950457	Date5 May 1995Decided	StatusActive

Official records

AccessGUDID record UDI-DI 20653405055393
FDA 510(k) database 510(k) number K950457

Across registries

2 registries list this device

FDA 510(k) K950457 decided 5 May 1995 Active
FDA GUDID UDI-DI 20653405055393 listed 24 Sep 2016 Listed

Timeline

2 dated events

5 May 1995 Cleared FDA 510(k) K950457
24 Sep 2016 Listed FDA GUDID 20653405055393

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Core Dynamics
Generic name: Laparoscopic access cannula, single-use
Model / Ref / Catalog: CD1935

Primary DI / UDI-DI: 20653405055393
510(k) Number: K950457
FDA product code: HET
GMDN term: Laparoscopic access cannula, single-use

Device class: Class II
Regulation number: 884.1720
GUDID distribution status: In Commercial Distribution

Sterilisation method: Ethylene Oxide

Size: Length — 100 Millimeter
Outer Diameter — 5 Millimeter

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

Supplied sterile
Sterilise before use
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (9, all answered No)