Identity
- Trade Name
- DBC Spring Ten FDA UDI
- Generic Name
- Acupuncture needle, single-use FDA UDI
- Device Name
- DBC Spring Ten Acupuncture Needles are high quality bulk packaged needles at an economical price. The DBC™ Spring Ten needle is manufactured in an automated facility, giving it consistency and quality unrivaled by other needles in the market. Sterile disposable, surgical stainless steel acupuncture needles with 25 mm "spring" style metal handle. 10 needles with 1 insertion tube per sterile bulk package. Box of 1000 needles. FDA UDI
- Model / Reference
- dSB.18x30 FDA UDI
- Description
- DBC Spring Ten Acupuncture Needles are high quality bulk packaged needles at an economical price. The DBC™ Spring Ten needle is manufactured in an automated facility, giving it consistency and quality unrivaled by other needles in the market. Sterile disposable, surgical stainless steel acupuncture needles with 25 mm "spring" style metal handle. 10 needles with 1 insertion tube per sterile bulk package. Box of 1000 needles. FDA UDI
Identifiers
- Catalog Number
- dSB.18x30 FDA UDI
- Primary DI / UDI-DI
- 18800018900281 FDA UDI
- 510(k) Number
- K990328 FDA UDI
- FDA Product Code
- MQX FDA UDI
- GMDN Term
- Acupuncture needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5580 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
Yes
FDA UDI
Category: Acupuncture needle, single-use
DBC Spring Ten by Dong Bang Medical co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Acupuncture needle, single-use.
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Cleared under the same submission
K990328 also covers:
- DBC Intradermal — Dong Bang Medical co., Ltd.
- DBC Intradermal — Dong Bang Medical co., Ltd.
- DBC Intradermal — Dong Bang Medical co., Ltd.
- DBC Pipe Single — Dong Bang Medical co., Ltd.
- DBC Pipe Single — Dong Bang Medical co., Ltd.
- DBC Pipe Single — Dong Bang Medical co., Ltd.
- DBC Pipe Single — Dong Bang Medical co., Ltd.
- DBC Pipe Ten — Dong Bang Medical co., Ltd.
- DBC Pipe Ten — Dong Bang Medical co., Ltd.
- DBC Pipe Ten — Dong Bang Medical co., Ltd.
- DBC Pipe Ten — Dong Bang Medical co., Ltd.
- DBC Pipe Ten — Dong Bang Medical co., Ltd.
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
- Dong Bang Medical co., Ltd.
Sources (1)
- FDA UDI 30707d5c-3b66-43cf-9647-bc9b7ba04852 37 fields · synced May 30, 2026