Tenoscope
FDA 510(k) K970642 · Luxtec Corp.
510(k) numberK970642
Submission
- Device name
- Tenoscope
- Applicant
- Luxtec Corp.
Newton, MA, US - Received
- February 20, 1997
- Decision date
- May 21, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- HRX – Arthroscope
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.1100
- Specialty
- Orthopedic
Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Other 510(k)s with product code HRX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260203 | Fule Vertebroplasty Balloon CatheterHRX · Traditional | Beijing Fule Science & Technology Development… | 08/28/2026SE |
| K254103 | HOPKINS Telescopes for ArthroscopyHRX · Traditional | Karl Storz SE & CO. KG | 08/26/2026SE |
| K252790 | Digital ClarusScope System and Digital NeuroPEN SystemHRX · Traditional | Clarus Medical, LLC | 05/26/2026SE |
| K253523 | Freedom DS Decompression SystemHRX · Traditional | Spinal Simplicity | 04/16/2026SE |
| K252546 | VantageTM Lumbar Decompression KitHRX · Traditional | Allevion Medical, LLC | 03/12/2026SE |
| K253217 | MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500)…HRX · Traditional | Medimaging Integrated Solution, Inc (Miis) | 12/23/2025SE |
| K250795 | Purevue FMSHRX · Traditional | W.O.M. World of Medicine GmbH | 12/05/2025SE |
| K252666 | Articulator Arthroscopic BurHRX · Traditional | Joint Preservation Innovations, LLC | 11/21/2025SE |
| K252458 | Kyphoplasty Balloon Dilatation CathetersHRX · Traditional | Shanghai Lange Medtech Co., Ltd. | 11/03/2025SE |
| K252020 | TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade AssemblyHRX · Traditional | Hand Biomechanics Lab, Inc. | 10/15/2025SE |
More from Hand Biomechanics Lab, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K973193 | LuxscopeHQF · Traditional | 11/21/1997SE |
| K970562 | TenosnareHRX · Traditional | 05/14/1997SE |
| K950960 | Reddy IlluminatorFFS · Traditional | 09/08/1995SE |
| K895248 | IMS5000 Illuminated LoupesFSP · Traditional | 09/15/1989SE |
| K890716 | Luxtec Aco Series 4000 Light SourceFCW · Traditional | 04/26/1989SE |
| K864387 | Luxtec Fiberoptic CablesEQH · Traditional | 05/22/1987SE |
| K864383 | Luxtec, Killian and Vienna Nasal SpeculumsEQH · Traditional | 01/14/1987SE |
| K864382 | Frazier Suction TubeEQH · Traditional | 01/14/1987SE |
| K864385 | Luxtec Light SourcesFCW · Traditional | 01/13/1987SE |
| K864865 | Speculum, Vaginal, Metal FiberopticHDG · Traditional | 01/09/1987SE |
Questions and answers
When was Tenoscope cleared by the FDA?
Tenoscope (K970642) received a 510(k) decision of Substantially Equivalent on May 21, 1997, 90 days after the submission was received.
What is the product code of K970642?
The FDA product code is HRX – Arthroscope, a Class II (moderate risk) device regulated under 21 CFR 888.1100.