Bioviva-3D Dental

Basik PGC SUTURE USP 3/0..3/8 REV CUTTING NEEDLE 24MM LENGTH One Device

Registry build 21.09.26
4manufacturers in China registered for this device type
5catalogue numbers in this listing

Who Else Makes It

Concentrated in Shanghai (1), Shandong (1), Beijing (1).

Chinese manufacturers registered for FDA product code GAM
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Sichuan Innovation Technology Co., Ltd. Chengdu Sichuan Contract manufacturer 2

Record

Regulatory record for Bioviva-3D Dental
Listed by 3D Dental Designs AND Development, LLC
FDA product code GAM
Device type Suture, Absorbable, Synthetic, Polyglycolic Acid
Device class Class 2
Regulation 21 CFR 878.4493
510(k) K130737
Record published 2016-12-15
Record revised 2021-02-05 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 12
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Bioviva-3D Dental
Catalogue number Size Status
BPGC942 In distribution
SPGC40 In distribution
BPGC987 In distribution
BPGC922 In distribution
BPCG943 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Novosyn B Braun Surgical SA 2,286
DemeCRYL Demetech Corp. 2,092
DemeSORB Demetech Corp. 1,625
Safil B Braun Surgical SA 1,613
Monosyn B Braun Surgical SA 1,096
E-Pack Ethicon, Inc. 967
Coated Vicryl Ethicon, Inc. 933
DemeQUICK Demetech Corp. 732
Polysorb Covidien LP 732
DemeCAPRONE Demetech Corp. 707
Wego-PGA Absorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 554
Safil Quick+ B Braun Surgical SA 414

Showing 12 of 463. All products under Suture, Absorbable, Synthetic, Polyglycolic Acid

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
P840051 1989-06-07 MAXON(TM) POLYGLYCONATE MONOFILAMENT ABSORBABLE SU Davis & Geck, Inc.
N18387 1987-06-18 PDS(TM) SUTURE (CLEAR) Ethicon, Inc.
N16881 1981-12-04 DEXON 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