What is FDA product code FDA?

To provide visualization and perform various procedures within the small intestine. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Ancora · Enteroscope and Accessories → Gastroenterology & Urology

Name: Ancora
Brand: Ancora

1manufacturer

1catalogue number

2510(k) clearances naming this product code

Who Else Makes It

Registered in Liaoning. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FDA
Manufacturer	City	Province	Registered as	Device types
Dalian Create Medical Products Co., Ltd.	Dalian	Liaoning	Contract manufacturer	2

Record

Regulatory record for Ancora
Listed by	Aspero Medical, Inc., United States
FDA product code	FDA
Device type	Enteroscope And Accessories
Device class	Class 2
Regulation	21 CFR 876.1500
Establishment	Complaint-file establishment, Manufacturer
510(k)	K231323
Record published	2023-10-26

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Single use	Yes
Prescription	Prescription only
Latex	Labelled latex-free
Label carries	lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Ancora
Catalogue number	Size	Per pack	Status
Ancora-SB 4-pack		4	In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Fujifilm	Fujifilm Corporation	6
Cardinal Health	Cardinal Health 200, LLC	2
Balloon Control Unit	Olympus Medical Systems Corp.	2
Q Urological Persistent Aguamedicina	Q Urological Corporation	2
Evis Exera II Small Intestinal Videoscope	Olympus Medical Systems Corp.	2
Endoscope Position Detecting Unit	Olympus Medical Systems Corp.	2
CD138 + Cyclin D1	Biocare Medical, LLC	1
HealthMart	Strategic Sourcing Services LLC	1
TG-98 LM Synea 400	W&H Dentalwerk Bürmoos GmbH	1
Zeus-P	Spinal Elements, Inc.	1
Jade PTA Balloon Dilatation Catheter	OrbusNeich Medical (Shenzhen) Co., Ltd.	1
Premier Jackson Improved Short Tracheostomy Tube	Premier Dental Products Co.	1

Showing 12 of 19. All products under Enteroscope And Accessories

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K260314	2026-05-01
K231323	2023-08-31

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Ancora