Perma-Hand

Blue Multifilament Twisted (Virgin Silk), Nonabsorbable Surgical Suture

Registry build 21.09.26
1manufacturer
4catalogue numbers in this listing
1recall

Who Else Makes It

Registered in Beijing.

Chinese manufacturers registered for FDA product code GAL
Manufacturer City Province Registered as Device types
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for Perma-Hand
Listed by Ethicon, Inc., United States
FDA product code GAL
Device type Suture, Absorbable, Natural
Device class Class 2
Regulation 21 CFR 878.4830
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
510(k) K946173
Record published 2021-05-31
Record revised 2026-03-31 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 24, box of 12

Catalogue Numbers

Catalogue numbers for Perma-Hand
Catalogue number Size Status
SA63T In distribution
W1782 In distribution
SA65T In distribution
SA64T In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeGUT Demetech Corp. 1,421
Softcat B Braun Surgical SA 338
Ethicon Ethicon, Inc. 231
Catgut B Braun Surgical SA 147
Chromic Gut Covidien LP 142
Plain Gut Covidien LP 68
Reli® Myco Medical Supplies, Inc. 63
Darby Dental Supply, LLC Darby Dental Supply, LLC 60
Atramat Internacional Farmacéutica S.A DE C.V 52
Sharpoint Surgical Specialties México, S. de R.L. de C.V. 46
Suture, Absorbable, Natural C P Medical Inc. 44
Chromic Gut Riverpoint Medical LLC 33

Showing 12 of 237. All products under Suture, Absorbable, Natural

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Perma-Hand
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Ethicon, Inc. 510(k) number 2015-05-08 Class II Labeling mix-ups Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because the labeling on the box and foil are incomplete. 1,922 units 2017-06-06

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
N14226 1987-08-28 ABSORBABLE SURGICAL SUTURE, USP Ethicon, Inc.
N10389 1987-06-18 ABSORBABLE SURGICAL SUTURE, USP Ethicon, Inc.
N84380 1985-02-27 PLAIN GUT SUTURES Deknatel, Inc.
N83038 1984-04-27 PLAIN GUT STERILE ABSORBABLE SUTURES Davis & Geck, Inc.
N83433 1983-08-18 CHROMIC GUT STERILE ABSORBABLE SUTURES Davis & Geck, Inc.
N84381 1981-08-11 GUT Deknatel, Inc.
N8536 1981-01-06 CATGUT SUTURE Ethicon, Inc.
N15405 1981-01-06 COLLAGEN SUTURE (PLAIN!CHROMIC) ABSORBABLE Ethicon, 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