Skip to content

Transidyne General Corp.

United StatesFDA applicant, unverified

Devices
21

What Transidyne General Corp. makes

Transidyne General Corp. manufactures medical devices including umbilical cord and fetal blood sampling kits, surgical tools like saw blades and burs, tracheostomy care supplies, and modular scanning densitometry systems. Their portfolio also covers procedural kits such as IV start and laceration trays, as well as specialized consumables like SQC buffers and prophylaxis packs.

The company’s devices are classified under FDA regulations as Class I and Class II, with many listed via the 510(k) pathway. These products are intended for use in clinical, surgical, and diagnostic settings, and the manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue21

Newest first, rows 1-21 of 21

Search and filter all 21 devices
Skip device list

  • Corometrics Medical Systems 220 Ph Sys. Ref K800271

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Model 1050 - Umbilical Cord Blood Sampling Kit Ref K897133

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Surgical Saw Blades Ref K950403

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Tracheostomy Care Kit Ref K924243

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Surgical Bur Ref K950449

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • I.V. Start Kit Ref K924811

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fetal Blood Sampling Kit Model 1560 Ref K810028

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Sqc Buffer Ref K812601

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Laceration Tray Ref K955658

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Modular Scanning Densitometer Sys. Ref K780318

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Fetal Blood Sampling Kit #1560 Ref K831459

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Prophylaxis Pack Ref K950773

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Oral Procedure Pack Ref K950743

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • 1400 Series Evidence Collection Kit Ref K896373

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bodily Fluid Disposal Kit Ref K961217

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Corometrics Medical Syst. 220 Ph Analy. Ref K812552

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • 1570 - Fetal Blood Sampling Kit Ref K891388

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • 1420 Heel-Stick(Tm) Neonatal Blood Sampling Kit Ref K895202

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Primary Surgical Dressing Tray Ref K922041

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Suture Removal Kit Ref K922339

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Corning 760 Fluorometer/Densitometer Ref K803240

    Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 1-21 of 21

Frequently asked questions

How many devices does Transidyne General Corp. have in the registry?

The registry currently lists 21 devices for Transidyne General Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Transidyne General Corp.'s devices?

Among its 21 most recently registered devices, Transidyne General Corp. has devices listed in FDA 510(k) (21 devices).

What risk classes do Transidyne General Corp.'s devices fall under?

Among its 21 most recently registered devices, the classes recorded for Transidyne General Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Transidyne General Corp. in the registry?

The most recently registered devices listed for Transidyne General Corp. include COROMETRICS MEDICAL SYSTEMS 220 PH SYS., MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT, SURGICAL SAW BLADES and TRACHEOSTOMY CARE KIT.

Generated automatically from registry data and not verified by a human reviewer.