Identity
- Trade Name
- Sterling Medical Products FDA UDI
- Generic Name
- Orthodontic archwire/bracket ligature FDA UDI
- Device Name
- STERILE RUBBER BANDS FDA UDI
- Model / Reference
- 546 FDA UDI
- Description
- STERILE RUBBER BANDS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00685404000346 FDA UDI
- GMDN Term
- Orthodontic archwire/bracket ligature FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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: Orthodontic archwire/bracket ligature
Sterling Medical Products by Apollo Medical Products Corp. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthodontic archwire/bracket ligature.
- SELECT-TIES — G&H Wire Company, Inc. · Class I
- AURADONICS — AURADONICS INC. · Class I
- Kobayashi Tie Hooks — RELIANCE ORTHODONTIC PRODUCTS, INC. · Class I
- 3M™ AlastiK™ — 3M UNITEK CORPORATION · Class I
- Mini Stix Ligature Ties — TP ORTHODONTICS, INC. · Class I
- MINI-TIES — Ortho Organizers, Inc. · Class I
- Plak Smacker — Young Innovations, Inc. · Class I
- PHOENIX — AURADONICS INC. · Class I
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Apollo Medical Products Corp.
Sources (1)
- FDA UDI fc821e47-6a5b-4b44-a0b6-c74eb428a80a 34 fields · synced Jun 1, 2026