Drill S-PI-A1.6

Drill for SF Push-in Anchor 1.6

Registry build 21.09.26
6manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Fujian (1).

Chinese manufacturers registered for FDA product code GAT
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38
Shandong Haidike Medical Products Co., Ltd. Heze Shandong Manufacturer 22
Xiamen Zhiyuan Medical Technology Co., Ltd. Xiamen Fujian Contract manufacturer 22
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for Drill S-PI-A1.6
Listed by Surgical Fusion Technologies GmbH, Switzerland
FDA product code GAT
Device type Suture, Nonabsorbable, Synthetic, Polyethylene
Device class Class 2
Regulation 21 CFR 878.5000
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K240288
Record published 2024-04-12
Record revised 2025-10-07 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Drill S-PI-A1.6
Catalogue number Size Status
Drill S-PI-A1.6 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Premicron B Braun Surgical SA 1,377
Deknatel Teleflex Medical LLC 1,198
FlexiGRAFT® LifeNet Health 992
DemeBOND Demetech Corp. 939
Ti-Cron Covidien LP 482
HS FIber Riverpoint Medical LLC 413
Ethibond Excel Ethicon, Inc. 383
Arthrex® Arthrex, Inc. 307
Dagrofil B Braun Surgical SA 195
WEGO-Polyester Nonabsorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 175
Cardioxyl ® Peters Surgical 162
Silkam B Braun Surgical SA 150

Showing 12 of 275. All products under Suture, Nonabsorbable, Synthetic, Polyethylene

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
N16374 1986-01-23 PROLENE*POLYPROPYLENE SUTURE NONABSORBABLE SURG. S Ethicon, Inc.
P810028 1984-12-17 DEKLENE(TM) Deknatel, Inc.
N17825 1981-09-24 SURGILENE Davis & Geck, Inc.

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer