Identity
- Trade Name
- EXOSHAPE FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 8 MM x 30 MM FDA UDI
- Model / Reference
- 1101-00-0830 FDA UDI
- Description
- EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 8 MM x 30 MM FDA UDI
Identifiers
- Catalog Number
- 1101-00-0830 FDA UDI
- Primary DI / UDI-DI
- 20653405986840 FDA UDI
- 510(k) Number
- K101808 FDA UDI
- FDA Product Code
- MBI FDA UDIHWC FDA UDI
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrical-only medical device connection cable, reusable
Exoshape by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical-only medical device connection cable, reusable.
- Unimed — Unimed Medical Supplies, Inc. · Class II
- Guenter Bissinger Medizintechnik GmbH — Günter Bissinger Medizintechnik GmbH · Class II
- Unimed — Unimed Medical Supplies, Inc. · Class II
- Symmetry Olsen — Olsen Medical · Class II
- Connection Cable — Shenzhen Keborui Electronics Co., Ltd · Class I
- TC-HEART LUNG DIN INTFC CA STOCKET — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- MICTEC CONNECTION CABLE — SONTEC INSTRUMENTS, INC. · Class II
- ECG Cable — Edan Instruments,Inc. · Class I
Cleared under the same submission
K101808 also covers:
- EXOSHAPE — Conmed Corporation
- EXOSHAPE — Conmed Corporation
- ExoShape — Medshape, Inc.
- ExoShape — Medshape, Inc.
- ExoShape — Medshape, Inc.
- ExoShape — Medshape, Inc.
- ExoShape — Medshape, Inc.
- ExoShape — Medshape, Inc.
- ExoShape — Medshape, Inc.
- ExoShape Teno — Medshape, Inc.
- ExoShape Teno — Medshape, Inc.
- ExoShape Teno — Medshape, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI ecc17e24-2759-4b47-8eb8-9858281544bc 37 fields · synced Jun 8, 2026